Otrivin Extra

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Otrivin Extra

Medically reviewed

Marina Burgos

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Otrivin Extra

Quick Facts

Property Description
Active Ingredients Xylometazoline Hydrochloride, Ipratropium Bromide
Form Aqueous Nasal Spray (Metered Dose)
Pharmacological Class Sympathomimetic and Anticholinergic
Common Use Concurrent symptomatic relief of nasal congestion and rhinorrhea
Origin Synthetic (both active compounds)

The Identity of Otrivin Extra: A Fixed-Dose Combination Nasal Spray

Otrivin Extra is defined as a medicinal product presented as a fixed-dose combination product intended for topical intranasal administration as an aqueous nasal spray. This unique product contains two distinct, synthetically derived active ingredients: Xylometazoline Hydrochloride and Ipratropium Bromide. This combination approach delivers two classes of medication in a single, measured dose, which generally distinguishes it from standard single-agent nasal decongestants. It is often positioned for the adult and adolescent patient group experiencing moderate-to-severe symptoms where both a blocked nose and a runny nose are present.


Active Ingredients and Pharmacological Class of the Formulation

The formulation is classified into two separate pharmacological classes: sympathomimetics and anticholinergics. Xylometazoline Hydrochloride acts as the decongestant, specifically an alpha-adrenergic agonist, inducing rapid vasoconstriction (narrowing of blood vessels) in the nasal mucosa. The second component, Ipratropium Bromide, is an anticholinergic agent that provides an antisecretory effect by inhibiting glandular signals. Pharmacological studies have clinically recognized this combination for its superior effect on nasal obstruction and discharge compared to placebo, confirming its dual-action utility.


General Purpose: Targeting Congestion and Rhinorrhea Concurrently

The general utility of the Otrivin Extra formulation is the concurrent symptomatic relief of two primary physical discomforts: nasal congestion (stuffy nose) and rhinorrhea (excessive watery runny nose). The fixed combination is designed to achieve a synergistic effect, allowing for simultaneous action against the vascular swelling that causes congestion and the glandular overactivity that causes discharge. This mechanism provides a comprehensive symptomatic approach that addresses both primary physical discomforts through local action within the nasal passages.

What side effects are possible with Otrivin Extra?

Possible Side Effects and Safety Information

The safety profile of the Xylometazoline/Ipratropium Bromide combination nasal spray is based on frequency classifications defined in regulatory documentation. Adverse reactions are primarily local, but potential systemic effects are documented.


Frequency-Classified Adverse Reactions

Classification Examples of Documented Effects
Very Common Nasal Dryness, Epistaxis (nosebleed)
Common Headache, Dry Mouth, Dysgeusia (altered taste), Rhinalgia (nose pain/discomfort)
Uncommon Palpitations, Tachycardia, Insomnia, Tremor, Eye irritation, Hypersensitivity reactions (e.g., skin rash)
Rare/Very Rare Hypertension, Arrhythmia, Systemic allergic reactions (e.g., Angioedema)

Systemic Safety Considerations

Adverse effects are categorized by the body system affected, including Respiratory, Nervous System, Cardiac, and Eye Disorders. Serious reactions are rare but include documented cases of Increased Intraocular Pressure and aggravation of Narrow-angle Glaucoma, particularly if the spray contacts the eyes. Systemic cardiovascular effects such as Hypertension and Arrhythmia are associated with the sympathomimetic component, Xylometazoline.

Population and Duration-Related Safety

Official labeling states the product is not recommended for use in children and adolescents under 18 years due to a lack of sufficient safety documentation. Caution is advised for patients with pre-existing conditions such as hypertension, cardiovascular diseases, and diabetes mellitus. Chronic or excessive use of the nasal decongestant component may lead to a duration-related adverse pattern called rebound congestion (rhinitis medicamentosa), characterized by increased nasal swelling after the product is stopped.

Overdose and Emergency Response

Overdose manifestations are primarily linked to the systemic effects of the Xylometazoline Hydrochloride component, even though the product is administered locally. Overexposure can initially present with signs such as dizziness, headache, perspiration, and drowsiness. Systemic overdose may escalate to severe symptoms affecting the central and cardiovascular systems. These serious manifestations include coma, convulsions (seizures), respiratory depression, hypothermia (severely lowered body temperature), bradycardia (slow heart rate), and hypertension (high blood pressure), which may be followed by hypotension (low blood pressure).

When to Seek Urgent Help

The official regulatory guidance mandates that anyone suspected of an overdose must seek urgent symptomatic treatment under medical supervision. Appropriate supportive measures should be initiated immediately, and observation of the individual for several hours is required to monitor for serious systemic effects. Treatment is strictly symptomatic, as no specific antidote is known for Xylometazoline intoxication. Small children and infants are documented to be more sensitive to toxicity than adults, carrying a heightened risk for severe outcomes like central nervous system depression. Procedures like administering activated charcoal or gastric lavage may be considered in management, dependent upon the administered dose.

Therapeutic Uses of Otrivin Extra

Quick Facts

  • Relieves Nasal Congestion associated with common colds.
  • Reduces Runny Nose (Rhinorrhea) symptomatic of the common cold.
  • Provides Symptomatic Relief for the dual discomforts of a blocked and running nose.

Main Uses and Therapeutic Benefits

Otrivin Extra is indicated for the symptomatic treatment of both nasal congestion and runny nose (rhinorrhea) associated with a common cold. The formulation works to relieve these dual symptoms. The component that targets nasal congestion functions as a decongestant, which helps reduce excessive swelling of the nasal mucosa, thereby clearing the nasal passages and facilitating easier breathing. The second component is an anticholinergic agent that specifically addresses the symptom of a runny nose by reducing nasal secretions.

This combination provides focused relief for the simultaneous presence of a blocked and running nose, offering symptomatic management during a cold. Consistent with safe usage guidelines, this medicinal product is used for a limited duration of up to seven days to minimize the risk of adverse reactions, such as rebound congestion.

Regulatory References

  1. HPRA therapeutic product information

Eligibility and Restrictions for Use

The eligibility for using Otrivin Extra (xylometazoline/ipratropium) is strictly defined by regulatory authorities based on age, pre-existing medical conditions, and physiological status.

Eligibility Scope

Age Group Regulatory Status
Adults (18–70 years) Permitted for labeled use.
Children and Adolescents (<18) Not Recommended (Contraindicated) due to insufficient data.
Older Adults (>70 years) Limited experience of use; caution is advised.

Absolute Contraindications

The medicine must not be used by populations with the following specific, officially documented conditions:

  • Known hypersensitivity to Xylometazoline, Ipratropium Bromide, or atropine-like substances.
  • Narrow-angle glaucoma (increased pressure in the eyes).
  • Rhinitis sicca (chronic dry nasal inflammation) or atrophic rhinitis.
  • Recent surgery that exposed the dura mater (e.g., trans-sphenoidal hypophysectomy).
  • Use with Monoamine Oxidase Inhibitors (MAOIs), or within 14 days of discontinuing such treatments.

Conditional Use and Restrictions

Use requires caution and medical advice for patients with conditions like hypertension, cardiovascular disease (including Long QT syndrome), diabetes mellitus, hyperthyroidism, prostatic hypertrophy, or difficulty urinating.

  • Pregnancy: Not recommended as a precaution due to the potential systemic vasoconstrictor effect of Xylometazoline.
  • Lactation: Use is only permitted under medical advice, as it is unknown if the active substances are excreted in breast milk.

These official rules establish that the medicine is primarily for adults who are free from the listed contraindications, with limited use in older adults and conditional use in certain chronic health conditions.

What should I know about interactions with other medicines?

Interactions with Other Medicines and Products

The officially documented interaction profile for the combination of Xylometazoline (sympathomimetic) and Ipratropium (anticholinergic) is structured around pharmacodynamic reinforcement and regulatory restrictions.

Documented Interaction Restrictions

Interaction Type Interacting Agent Class Regulatory Constraint and Outcome
Sympathomimetic Reinforcement Monoamine Oxidase Inhibitors (MAOIs) Contraindicated due to risk of severely elevated blood pressure.
Sympathomimetic Reinforcement Tri-cyclic and Tetra-cyclic Antidepressants Use with caution; potential for reinforcement leading to elevated blood pressure.
Additive Anticholinergic Effect Other Anticholinergic Drugs Potential for additive systemic anticholinergic effects.

Timing and Population Notes

A mandatory timing rule requires that this medicinal product must not be used concurrently with MAOIs, or within 14 days of stopping MAOI treatment.

The profile includes population-specific considerations. Caution is advised regarding co-administration with beta-2 agonists in patients with a history of angle-closure glaucoma due to the Ipratropium component. Caution is also noted for patients with prostatic hypertrophy or bladder neck obstruction if they are receiving an anticholinergic by another route.

This structure reflects the regulatory focus on documented pharmacodynamic interactions, specifically the risk of cardiovascular effects from the sympathomimetic component and additive anticholinergic risks.

Mechanism of Action

Otrivin Extra utilizes a dual-action mechanism targeting alpha-adrenergic and muscarinic receptors. The component Xylometazoline functions as a selective alpha1-adrenergic receptor agonist. It acts upon alpha-adrenergic receptors in the nasal mucosa, triggering a G-protein-coupled intracellular cascade that ultimately leads to smooth muscle contraction and subsequent vasoconstriction within the nasal microvasculature. This reduction in vascular diameter decreases local blood flow and results in a decrease in tissue volume.

The second component, Ipratropium Bromide, acts as a muscarinic receptor antagonist. It selectively binds to muscarinic receptors, primarily the M2 and M3 subtypes, which are highly expressed on the serous and seromucous glands within the nasal passages. This competitive antagonism effectively blocks the cholinergic signaling pathway, consequently reducing the exocrine secretion of watery nasal fluids from these glands.

The overall mechanism of action results from the simultaneous operation of these two distinct pharmacological pathways: localized vasoconstriction (sympathetic-driven) and reduced glandular output (parasympathetic-modulated).

Dosage and Administration Information

How Otrivin Extra is Used: Official Administration Guidelines

Otrivin Extra (Xylometazoline Hydrochloride and Ipratropium Bromide) is administered through topical intranasal administration as an aqueous nasal spray, solution (metered dose). This fixed-dose combination requires specific adherence to guidelines regarding dosing, frequency, and duration of use, which are based on the official prescribing information.


Standard Dosing and Frequency

The standard regimen for adults (18 years and older) involves administering one puff in each nostril. Each metered application delivers a specified dose of 70 micrograms of Xylometazoline HCl and 84 micrograms of Ipratropium Bromide. The product may be used up to 3 times daily as needed, but a minimum interval of 6 hours must elapse between any two doses. The total dosage must not exceed 3 applications daily into each nostril.


Duration and Preparatory Use

Treatment duration should not exceed 7 consecutive days, and the principle of using the lowest effective dose for the shortest possible duration is emphasized. Users are recommended to discontinue use as soon as symptoms diminish. Before initial use, the pump must be primed with 4 to 5 actuations, and must be re-primed if it has been unused for longer than 6 or 7 days. If a full spray is not successfully administered, the dose is not to be repeated immediately.


Population and Procedural Rules

This product is not recommended for use in children and adolescents below 18 years of age due to lack of documentation. For procedural constraints, the nose should be cleared prior to administration, and the spray should only be used by one person to prevent the spread of infection. Users must avoid spraying the product in or around the eye.

Recent Clinical Evidence

Evidence for Use in Common Cold Symptoms

Clinical research on the combination of Xylometazoline Hydrochloride and Ipratropium Bromide (Otrivin Extra) primarily relies on short-term, randomized controlled trials (RCTs). These studies were designed to explore how this formulation was evaluated in people experiencing the simultaneous outcomes related to physical discomfort and rhinorrhea during an acute common cold. Researchers used these trials to examine patient-reported experiences, specifically by tracking outcomes related to the perceived intensity of nasal congestion and rhinorrhea throughout the study periods.

In these research settings, studies consistently monitored how symptoms evolved in the observed adult populations when compared against a neutral substance (placebo). Findings describe patterns observed in the studies that monitored physiological strain or stress related to these dual outcomes over defined time intervals. The evidence is relevant in studies examining symptom intensity or variability during the heightened symptom activity of a common cold.


Comparing the Combination Against Single-Ingredient Treatments

Research has explored how the fixed-dose combination nasal spray was evaluated in trials that compared it not only to placebo but also to its individual active ingredients—the decongestant alone and the anti-secretory agent alone. This comparison was evaluated in trials assessing short-term or episodic symptom patterns.

Findings indicate that studies monitored differences in patient-reported outcomes describing perceived discomfort. Research examined outcomes related to physical discomfort in conditions where symptoms may vary in intensity. Research describes changes measured during the study period when using the combination versus the single components. These findings describe group patterns and contribute to the broader evidence landscape related to the short-term outcomes of congestion and discharge.


Long-Term Research and Follow-up Duration

The body of evidence for the combination nasal spray focuses heavily on short-term follow-up because the product was studied for use during an acute episode. The main clinical studies generally observed responses over defined time intervals, typically reflecting a duration of up to seven days. This focus aligns with conditions characterized by acute or disruptive episodes.

There is limited information for long-term outcomes, and long-term effects are not fully established. Research provides insight into short-term changes but evidence is limited regarding sustained changes or effects beyond the period when the product was actively observed in studies. The certainty remains low regarding effects beyond the defined follow-up durations.


Evidence in Specific Patient Populations

The clinical research base primarily was evaluated in previously healthy adults (over 18 years of age) with acute symptoms of the common cold. Consequently, the results apply only to the populations studied and for the specific conditions presenting with cycles of stability and flare-ups.

Data for certain groups remain insufficient. For instance, there is a recognized lack of comprehensive evidence for the use of this fixed combination in older adults or individuals who have pre-existing medical conditions (comorbidities). Furthermore, data for adolescents and children was observed in some studies but is limited. Research provides context but not individual predictions for these groups, and study results reflect the specific conditions under which they were conducted.


Research Gaps and Areas of Uncertainty

Research has explored short-term symptom changes relevant in trials assessing short-term or episodic symptom patterns; however, several key limitations remain. The follow-up durations were limited, confining the evidence to acute use.

Additionally, the narrow population focus results apply only to the populations studied, and evidence derived from settings with varying symptom burdens is limited. Comparative evidence is lacking for all available therapeutic options, and findings reflect group patterns, not personal outcomes. Research contributes to the broader evidence landscape but evidence highlights what is known—and what is still uncertain.

Key Studies & References

  1. HPRA Medicines Information (General Product Search)
  2. HPRA Product Information Leaflet for Xylometazoline/Ipratropium (Otrivin Extra)

Frequently Asked Questions (FAQ)

Common questions about Otrivin Extra (FAQ)


Q: What happens if someone uses Otrivin Extra more often than described in the patient leaflet?

According to regulatory warnings, chronic use of the medicine, particularly the xylometazoline component, may lead to an increase in nasal lining swelling. This is known as a 'rebound effect' or rhinitis medicamentosa. This potential localized adverse reaction is why the official documents indicate a maximum recommended duration of use.


Q: Can Otrivin Extra cause something called 'rebound congestion'?

The potential for a 'rebound effect' or rhinitis medicamentosa is described in official documents as a risk associated with chronic use. This reaction is a swelling of the nasal lining that can occur if the product is used chronically or for longer than the prescribed maximum duration.


Q: Is 'rebound congestion' a commonly reported effect with this type of medicine?

The regulatory restriction that limits use to a maximum of 7 consecutive days is in place to minimize the risk of the 'rebound effect'. This restriction is consistent with the product's classification and is designed to address the potential for this known effect associated with the xylometazoline ingredient.


Q: What is the main difference between Otrivin Extra and regular Otrivin?

Otrivin Extra Dual Relief contains two different active components. While regular Otrivin typically includes only the decongestant (Xylometazoline), the 'Extra' version combines Xylometazoline with Ipratropium Bromide. This dual formulation is officially described as providing symptomatic relief for both nasal congestion and a runny nose (rhinorrhoea).


Q: Does Otrivin Extra have a different active ingredient than other nasal sprays?

Yes, this product is a fixed combination that contains two active substances: Xylometazoline Hydrochloride and Ipratropium Bromide. The combination is described as having a dual-action mechanism to target both nasal congestion and rhinorrhoea.


Q: How quickly should I expect to feel relief after using Otrivin Extra?

Product information indicates that the decongestant effect from the xylometazoline component is often felt within a few minutes of application. Studies have shown that relief may begin very quickly after use.


Q: What is the typical length of time the effects of Otrivin Extra are described to last?

The official product information describes the duration of action for the decongestant component as lasting for up to 10 hours.


Q: What are the most common reported safety issues or side effects of Otrivin Extra?

The most commonly reported safety issues described in the official product safety profile are nasal dryness and epistaxis, which is the medical term for nasal bleeding. Many effects described in the safety profile are reported as non-serious and temporary in nature.


Q: Are there any specific severe side effects mentioned in regulatory documents for Otrivin Extra?

Regulatory documents list certain effects as rare or very rare, including serious hypersensitivity reactions. These can involve symptoms like swelling (angioedema), rash, itching, or, rarely, serious effects concerning the cardiovascular or nervous systems.


Q: Does using Otrivin Extra affect my heart rate or blood pressure?

Official warnings advise caution for individuals sensitive to adrenergic substances, as these may potentially affect heart rate or blood pressure. This is particularly relevant for those with existing cardiovascular conditions or hypertension.


Q: Can individuals with certain existing medical conditions, like high blood pressure, use Otrivin Extra?

Official documents indicate the product should be used with caution for people with certain medical conditions, such as hypertension (high blood pressure), cardiovascular disease, hyperthyroidism, and diabetes mellitus. Caution is applied due to the potential systemic effects described for the decongestant component.


Q: Is Otrivin Extra considered a decongestant, an antihistamine, or both?

The product is classified as a combination of two types of medicine. Xylometazoline is a decongestant, and Ipratropium Bromide is an anticholinergic that works to dry up nasal secretions. It is officially classified as a decongestant and an anticholinergic agent, but it does not contain an antihistamine.


Q: Does Otrivin Extra interact with medications for depression or anxiety?

Official warnings state that using Otrivin Extra with certain medications, such as Monoamine Oxidase Inhibitors (MAOIs) or tri- and tetra-cyclic antidepressants, is not recommended. This combination carries a regulatory warning concerning the potential for severely elevated blood pressure.


Q: What research evidence exists for the combination of ingredients in Otrivin Extra?

Clinical studies described in regulatory documents demonstrated that the combination of xylometazoline and ipratropium bromide is effective. The evidence supports its regulatory classification for the relief of both nasal congestion and a runny nose associated with the common cold.


Q: Are there any official warnings about using Otrivin Extra during pregnancy?

Regulatory bodies advise against using this product during pregnancy. This caution is based on the potential for the decongestant component to cause a systemic vasoconstrictor effect (narrowing of blood vessels).


Q: What information is available regarding the use of Otrivin Extra while breastfeeding?

There is insufficient regulatory data to definitively confirm whether the product is transferred into breast milk. Due to limited regulatory data regarding excretion, official documents advise consultation with a healthcare professional before use while breastfeeding.


Q: Can Otrivin Extra cause dry nose or throat?

Nasal dryness is listed in the safety profile as one of the most common adverse reactions reported by users. Dryness in the mouth or throat has also been reported as a common effect.


Q: Is the sensation of a burning or stinging nose described as a common effect of Otrivin Extra?

Nasal discomfort, which includes sensations like burning or stinging, is listed as a common undesirable effect in regulatory documents. This is typically a localized and temporary sensation.


Q: Does Otrivin Extra affect my sense of smell or taste?

Alterations to taste sensation, or taste perversion, are listed as a possible adverse effect. The official documentation does not indicate that the product generally impairs the normal function of the nasal lining's cells.


Q: What evidence is there about the effectiveness of the two-ingredient formula?

The efficacy is described in regulatory documents based on clinical studies. The combination is described as providing effective relief for two primary symptoms of the common cold: a blocked nose (nasal congestion) and a runny nose (rhinorrhoea).


Q: Are there any known issues regarding people with glaucoma and Otrivin Extra?

The product is formally contraindicated for use by individuals with narrow-angle glaucoma. This is because the anticholinergic component (ipratropium) could potentially aggravate this condition if it contacts the eyes.


Q: Why are people with prostate issues sometimes advised against using decongestants?

The decongestant component is the basis for the caution indicated for individuals with conditions such as an enlarged prostate (hypertrophy of the prostate) or stenosis of the bladder. These conditions are sensitive to the systemic effects of decongestants.


Q: Is the onset of action described as immediate or delayed?

Product information for the decongestant component describes the onset of action as rapid. The effect is generally reported to begin within a few minutes after administration.


Q: Does Otrivin Extra contain preservatives or other inactive ingredients that might cause a reaction?

Yes, the product contains a full list of inactive ingredients, or excipients, which are detailed in the regulatory documentation. Hypersensitivity (an allergic reaction) to any of these listed inactive ingredients is a contraindication to using the product.


Q: What do official sources say about the potential for addiction with this product?

Official regulatory assessment reports state that the active ingredients, Xylometazoline and Ipratropium Bromide, are not known to have an abuse potential or lead to physical dependence or addiction.


Q: Can Otrivin Extra be used to help with sinus pressure or pain?

The decongestant component is officially indicated for the relief of nasal congestion. It is also described as an adjuvant, or assisting agent, to help with the drainage of secretions in conditions that affect the sinuses.


Q: Is it possible to develop a tolerance to the effects of Otrivin Extra?

The regulatory guidance requiring the product be used for no more than 7 consecutive days is designed to address the potential for a diminished effect and a localized adverse reaction (rebound effect) that can be associated with chronic use.


Q: What if the product does not seem to be working for my symptoms after a few days?

Regulatory guidelines indicate that if symptoms worsen, persist for longer than 7 days, or have not diminished after 3 days of treatment, an evaluation by a healthcare professional is warranted. This aligns with the principle of using the lowest effective dose for the shortest time.


Q: What does the research say about potential side effects on the nervous system?

Undesirable effects affecting the nervous system are listed in the safety profile. Headache is listed as a common effect, and other effects, such as dizziness or visual disturbances, have been reported in rare cases.


Q: Are there any official warnings for people who operate machinery after use?

Official warnings describe that activities requiring full attention, such as driving or operating machinery, may need to be avoided if a person experiences specific reported adverse effects like visual disturbances or dizziness.


Q: Can the ingredients in Otrivin Extra trigger a migraine or headache?

The safety profile lists headache as a common undesirable effect. However, the regulatory documents do not specify whether the product triggers migraines.


Q: What is the official information regarding overdose symptoms?

The official overdose section states that symptoms may include severe dizziness, sweating, and a severely lowered body temperature. Additionally, serious effects on the heart rate, impaired breathing, or convulsions have been reported.


Q: Is it normal to feel a brief dryness in the mouth or throat after using Otrivin Extra?

Dry mouth and dry throat have been reported as adverse effects. This is a common effect related to the action of the ipratropium bromide component.


Q: What is the description of the purpose of Otrivin Extra in official documents?

The official therapeutic indication for the product is the symptomatic treatment of both nasal congestion (blocked nose) and rhinorrhoea (runny nose). This is specifically in connection with having a common cold.


Q: Is Otrivin Extra classified as an opioid or does it contain any controlled substances?

Regulatory documents indicate that the active ingredients are not known to have abuse potential, and the product is not classified as an opioid or a controlled substance. It is classified as a medicine available only through a pharmacy.


Q: What should I know about the safety classification of Otrivin Extra?

In several countries, Otrivin Extra Dual Relief is classified as a Pharmacy (P) medicine. This classification means the product is distributed through a pharmacy and is generally sold by or under the supervision of a pharmacist.


Q: Do studies describe the safety profile of Otrivin Extra in children?

Official documents state that the product is not recommended for use in children and adolescents below 18 years of age. This is based on the lack of sufficient regulatory documentation regarding the safety and effectiveness of the product in this age group.


Q: Can Otrivin Extra be used by people who have recently had nose surgery?

The product is formally contraindicated for use by patients who have undergone certain types of recent nasal surgery. This includes procedures where the dura mater was exposed, such as trans-sphenoidal hypophysectomy.


Q: Is there any specific information about Otrivin Extra's effects on the eyes?

Contact with the eyes should be avoided, as it can cause temporary blurred vision, irritation, or red eyes, and may aggravate narrow-angle glaucoma. Users are instructed to avoid spraying the product near the eyes.

How should Otrivin Extra be stored and disposed of?

Storage and Disposal Requirements

Official regulatory guidelines define specific conditions for the safe storage and disposal of this medicine, ensuring stability and environmental protection.

Storage Conditions

Requirement Specifics Based on Labeling
Temperature Do not store above 25 C (room temperature); Do not freeze.
Protection Keep in the original container, protected from heat, light, and moisture.
Stability Discard 28 days after first opening. Do not use after the stated expiry date.
Safety Keep the medicine strictly out of the sight and reach of children.

Disposal Instructions

Medicines should not be disposed of using household waste or wastewater. For environmental safety, unused or expired product must be returned to a pharmacist or a designated collection point. This follows official environmental protection measures for pharmaceutical waste.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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