Metrocreme

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Medically reviewed

Marina Burgos

Last updated on 10/01/2026

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 Metrocreme

What is Metrocreme?

Metrocreme is a topical dermatological medication containing the active ingredient metronidazole. It is formulated as a cream specifically designed for application to the skin to manage the inflammatory symptoms associated with certain chronic skin conditions.

Therapeutic Class and Mechanism

Metronidazole, the primary component of Metrocreme, belongs to the nitroimidazole class of medications. While metronidazole is widely recognized for its antibacterial and antiprotozoal properties when taken systemically, its function in a topical cream format is primarily focused on its anti-inflammatory and antioxidant effects.

When applied to the skin, Metrocreme helps to reduce the redness, swelling, and the appearance of inflammatory lesions, such as papules and pustules. The exact mechanism by which it achieves these results in skin conditions is not fully understood, but it is believed to involve the suppression of reactive oxygen species and the modulation of the local immune response.

Primary Indications

Metrocreme is most commonly utilized in the management of rosacea, a long-term skin condition that typically affects the face. Rosacea is characterized by episodes of facial flushing, persistent redness, and the development of small, red, pus-filled bumps.

Unlike oral antibiotics, the topical application of metronidazole allows for the delivery of the medication directly to the affected areas, minimizing systemic absorption. It is intended for the treatment of inflammatory lesions rather than the non-inflammatory components of skin conditions, such as dilated blood vessels (telangiectasia).

Characteristics of the Formulation

As a cream-based vehicle, Metrocreme provides an emollient effect, which may be beneficial for patients who experience skin dryness or sensitivity. The formulation is designed to be easily absorbed into the skin layers while maintaining a protective barrier. It is typically white to off-white in appearance and is formulated to be non-greasy to facilitate regular application on facial skin.

Regulatory References

  1. National Institutes of Health (NIH) authoritative database

What side effects are possible with Metrocreme?

Possible side effects and safety information

The safety profile of topical metronidazole (Metrocreme) is largely characterized by localized reactions, which are classified by regulatory authorities based on frequency observed in clinical studies. The majority of reported adverse reactions fall within the Skin and Subcutaneous Tissue Disorders system-organ class.

Adverse Reactions and Frequency Classification

Adverse reactions that are officially documented as Very Common (affecting 10% or more of patients) typically involve local sensations and changes, such as dryness, scaling, pruritus (itching), and stinging at the application site. Reactions classified as Common (affecting 1% to 10% of patients) include generalized skin discomfort, erythema (redness), and instances of rosacea symptom worsening or contact dermatitis.

Less frequently, reports related to other systems, such as the Nervous System and Gastrointestinal Disorders, have been documented, including metallic taste and nausea.

Serious Safety Considerations

A serious adverse reaction, Peripheral Neuropathy (characterized by numbness, tingling, or paresthesia), has been reported in post-marketing surveillance for topical metronidazole. The official label advises caution for patients with a history of blood dyscrasia and explicitly contraindicates the medication in individuals with a history of hypersensitivity to metronidazole or any component of the cream.

Population-Specific Safety Notes

Regulatory documents state that the safety and effectiveness have not been established in pediatric patients. For pregnant or breastfeeding women, the official prescribing information requires careful consideration, noting the classification of Pregnancy Category B and the known secretion of the drug into human milk following oral use.

Overdose and Emergency Response

Overdose and when to seek help

Official regulatory information indicates that overdose from the intended topical application of Metrocreme is considered unlikely due to the minimal systemic absorption of the active ingredient, metronidazole, through the skin. For this reason, regulatory labels do not document specific clinical signs or symptoms resulting from excessive use on the skin.

Required Emergency Actions

The primary concern and regulatory focus is the risk of accidental ingestion of the cream. If a large amount of Metrocreme is accidentally swallowed, official guidance mandates that you seek immediate medical attention or contact a poison control center right away.

Overdose Context Official Regulatory Statement
Risk Classification Overdose is classified as low or unlikely for the intended topical route.
Antidote Availability No specific antidote is known for metronidazole overdose.
Management Treatment is officially defined as symptomatic and supportive.

This profile defines the sole condition—accidental ingestion—under which regulatory authorities mandate that urgent medical help must be sought. Management and monitoring are focused on observation for systemic effects that may occur following oral exposure.

Therapeutic Uses of Metrocreme

What Metrocreme treats: main uses and benefits

Topical Metronidazole is considered relevant for the long-term management of chronic inflammatory rosacea, its primary therapeutic domain. This medication is used for managing the recurrent, visible manifestations of the disease, including persistent facial redness, inflammatory papules, and pustules. The preparation is relevant across domains where supportive symptomatic support is needed, contributing to easing the overall symptom load when symptoms may become disruptive during flare-ups.

It is applied in addressing symptom clusters that may become intense, such as the appearance of inflammatory red bumps. Addressing these clusters may assist with maintaining functional stability and contributes to easing the overall symptom load during periods of heightened discomfort.

“The medication is commonly used to help with episodes marked by increased discomfort, contributing to easing the overall symptom load associated with recurrent inflammation.”

It is relevant for easing the intensity of persistent facial redness (erythema), which may help patients cope more steadily with symptom fluctuations when symptoms are more noticeable, assisting with maintaining functional stability.


Quick Fact: Relief for Inflammatory Skin Symptoms

This medication is considered relevant for long-term topical treatment, playing a role in managing the appearance and intensity of inflamed lesions and the associated redness characteristic of chronic facial skin conditions.

Regulatory References

  1. NIH MedlinePlus Drug Information

Eligibility and Restrictions for Use

The official regulatory profile for Metrocreme (topical metronidazole) strictly defines eligibility for use, outlining populations who are permitted, restricted, or prohibited from using the medicine. Use is authorized for adult patients with the inflammatory lesions of rosacea.

Absolute Contraindications

The medicine is contraindicated in individuals with a history of hypersensitivity (allergic reaction) to metronidazole, other nitroimidazole derivatives, or any inactive ingredient in the formulation. Some international labeling also lists Cockayne syndrome as an exclusion criterion.

Age and Physiological Restrictions

Category Regulatory Status
Pediatric Patients Safety and effectiveness have not been established, rendering use in children and adolescents officially non-recommended.
Older Adults Use is generally acceptable, though regulatory documents caution that greater sensitivity in some older individuals cannot be ruled out.
Pregnancy Use is restricted to being only if clearly needed (Category B), as metronidazole crosses the placental barrier.
Lactation A decision must be made to either discontinue nursing or discontinue the drug, weighing the importance of the drug to the mother.

Conditional Use Warnings

Due to the nature of the nitroimidazole class, the drug should be used with care in patients with a history of blood dyscrasia (blood cell disorders) and administered with caution to patients with central nervous system diseases.

What should I know about interactions with other medicines?

The official interaction profile for Metrocreme (Metronidazole topical) is structured by the systemic interaction risks established for its active ingredient, Metronidazole, requiring specific caution despite the low systemic absorption from skin application. The regulatory documentation highlights interactions in the following domains:

Interaction Category Documented Entity Official Constraint or Outcome
Exposure Modification Oral Anticoagulants (Warfarin) Potentiation of the anticoagulant effect, requiring careful monitoring of prothrombin time (INR).
Pharmacodynamic Risk Alcohol (Ethanol) Risk of disulfiram-like reaction, necessitating avoidance of alcohol-containing products.
Timing Rule Alcohol Mandatory avoidance during therapy and for at least 48 to 72 hours after the last dose.

Official Interaction Statements:

  1. Interaction with Oral Anticoagulants: Official documents note that Metronidazole can potentiate the anticoagulant effect of medicines like Warfarin, resulting in a prolongation of prothrombin time. Caution and careful monitoring are explicitly required when the topical cream is co-administered with these agents.
  2. Interaction with Alcohol: The risk of a disulfiram-like reaction necessitates that alcohol-containing products must be avoided during therapy and for a regulatory period of at least 48 hours after discontinuation. The interaction pattern involving Disulfiram itself is also noted as a risk for the active ingredient.

This profile is formally structured by these risks to guide prescribing and monitoring, as documented in the FDA Prescribing Information and analogous national regulatory monographs.

Mechanism of Action

The mechanism of metronidazole involves two distinct biological systems: the inflammatory pathway and the microbial environment.

Modulation of Localized Inflammatory Responses

This domain focuses on the anti-inflammatory mechanism, which is relevant to the modulation of localized tissue reactions. The drug engages mechanisms that influence immune cell signaling. Specifically, it affects the function of neutrophils, the primary inflammatory cells, by reducing the generation of highly reactive molecules, known as reactive oxygen species (ROS). This action influences the degree of oxidative stress at the tissue level, leading to a modulation of localized fluid dynamics and microvascular tone.

Selective Antimicrobial Bioactivation

This domain addresses the fundamental antimicrobial property of metronidazole. The drug, an inactive prodrug, is selectively activated only by anaerobic microorganisms (e.g., certain bacteria and protozoa) in a low-oxygen environment. This reductive bioactivation creates highly reactive intermediate radicals that target and disrupt the organism’s DNA helical structure. This mechanism leads to the physiological outcome of selective microbial elimination (cytotoxicity), which results in the modulation of microbial components that influence localized inflammatory reactions.

Dosage and Administration Information

The administration of Metronidazole Topical Cream 0.75% is defined by instructions that govern the specific application route, frequency, and required preparation. Adherence to this guidance is necessary to ensure the medication is used strictly according to the product label.


Administration Scope: Official Guidelines

The mandated route of administration for this preparation is strictly topical, intended only for application to the affected skin area. The cream is explicitly not approved for ophthalmic (eye), oral, or intravaginal use.

The labeled dosing schedule requires applying a thin layer of the 0.75% cream and gently rubbing it into the entire area designated for treatment. The required frequency of use is twice daily (B.I.D.), typically scheduled for one application in the morning and one in the evening.


Pre-Application Conditions

The protocol requires certain preparation requirements before each application: the treated skin area must be cleansed with a mild wash. As a special procedural condition, patients may apply cosmetics or makeup to the treated area after the cream has been fully applied and absorbed. Furthermore, the label directs that the application must strictly avoid contact with the eyes.


Connection to Protocol

These instructions define a standardized, external application protocol that requires consistency in frequency, pre-application cleansing, and adherence to the specified route. This protocol structures the approach to using the medicine over the typical treatment course length.

Recent Clinical Evidence

Metrocreme: Recent Clinical Evidence

Evidence for Use in Inflammatory Lesions of Rosacea

Research explored the study design involving metronidazole cream primarily utilized Randomized Controlled Trials (RCTs), often designed as double-blind, vehicle-controlled studies. These trials were used in research exploring how symptoms change over time, typically including adult patients (age ge 18 years) with rosacea characterized by inflammatory papules and pustules. The research examined outcomes linked to inflammatory or irritative states, focusing on measuring the number of inflammatory lesions and assessing overall disease status using the Investigator's Global Assessment (IGA) score. Studies report how symptoms evolved in the observed populations, noting patterns related to changes in lesion counts when compared against the non-medicated control cream. Findings describe patterns observed in the studies, including the percentage of participants reaching a specific threshold on the IGA scale. This evidence contributes to understanding symptom patterns, often measured alongside the condition's impact on daily life.

Research on Related Symptoms (Facial Redness and Vascular Components)

Alongside the primary measures, studies also examined the severity scoring of persistent facial erythema (redness), a measure applied in research contexts involving fluctuating or unstable symptoms. Evidence so far indicates limited data for assessing symptom change in persistent facial erythema when assessed as a primary outcome. Furthermore, research describes that studies focusing on the vascular component, such as thread veins (telangiectasia), was not associated with a measured change in the observed populations. Research highlights that changes measured during the study period were predominantly confined to the inflammatory outcomes related to physical discomfort.

Long-Term Evidence and Durability of Effect

The initial efficacy studies for metronidazole cream were conducted during periods of increased symptom activity and research explored short-term symptom changes, with follow-up durations typically lasting between 7 and 12 weeks. To understand sustained response, maintenance studies were conducted, observing responses over defined time intervals, sometimes extending up to 6 months or 36 weeks.

Studies in Specific Patient Groups

Studies primarily monitored adult populations presenting with conditions where symptoms may vary in intensity. Research examined outcomes reflecting daily functioning or activity level across different severity strata; many pivotal trials focused on the moderate to severe presentation of papulopustular rosacea. However, data for certain groups remain insufficient. For instance, appropriate studies regarding the relationship of age to effects were not evaluated in the pediatric population. This means available research data are insufficient for individuals younger than 18, and findings describe group patterns applicable primarily to the adult populations studied.

Research Gaps and Unstudied Areas

Long-term effects are not fully established, as follow-up durations were limited in the core regulatory trials, meaning there is limited information for long-term outcomes related to usage over several years. Evidence highlights what is known—and what is still uncertain—particularly regarding the study outcomes for non-inflammatory symptoms like facial redness. The research does not determine whether an individual will respond similarly to the group patterns observed, as study results reflect the specific conditions under which they were conducted. Comparative evidence is lacking for some comparison scenarios.

Key Studies & References Metronidazole Topical Gel USP, 0.75% Clinical Pharmacology and Indications (DailyMed)

Frequently Asked Questions (FAQ)

Common questions about Metrocreme (FAQ)


Q: Can Metrocreme cause my skin to feel dry or irritated?

A: Official regulatory documents describe skin dryness and irritation as commonly reported localized reactions. Reactions like dryness, scaling, itching (pruritus), stinging, and skin discomfort are frequently documented in the product's official safety information.


Q: Is it normal to feel a stinging sensation when I first apply Metrocreme?

A: A stinging sensation at the application site is officially classified as a Very Common adverse reaction in the drug’s labeling. This means it is an event observed in a significant number of patients using the cream.


Q: What should I do if I accidentally get Metrocreme in my eyes?

A: Regulatory information advises that contact with the eyes should be strictly avoided because it has been reported to cause tearing. Regulatory guidance for accidental eye contact generally suggests rinsing the area with water.


Q: Can Metrocreme be used by children?

A: Official prescribing information states that the safety and effectiveness of this medication have not been established in the pediatric population (individuals under 18 years of age). This means there is insufficient data to support use in this age group, and the drug is not generally recommended for children.


Q: How long does a tube of Metrocreme typically last?

A: Metrocreme is commonly supplied in a 45-gram tube. Based on typical prescribing and supply patterns, a 45-gram tube is often intended to last around 25 days, but the actual duration will depend on the area being treated.


Q: Does Metrocreme help with the redness or just the pimples/bumps of rosacea?

A: The drug is officially indicated for the treatment of the inflammatory papules and pustules (the pimples and bumps) of rosacea. While the medication has anti-inflammatory properties, research evidence indicates there is limited data available to formally assess changes in persistent facial erythema (redness) as a primary outcome.


Q: Is there a maximum amount of time Metrocreme is generally used for?

A: Regulatory trial evidence for efficacy was observed over initial periods of up to 12 weeks, with follow-up and maintenance studies extending up to 6 months or 36 weeks. A specific, official maximum duration of continuous therapy is not defined in the product label.


Q: What if I experience mild burning after applying Metrocreme?

A: Burning and stinging at the application site are officially documented as common reactions. Official labeling notes that if local irritation is experienced, patients may need to review the situation with their prescriber to consider adjustments to the frequency of application or discontinuation.


Q: Is Metrocreme the same as generic metronidazole cream?

A: Metrocreme is a specific brand name for the active ingredient metronidazole topical cream, 0.75%. The FDA has determined that generic versions of the 0.75% cream are bioequivalent and therapeutically equivalent to the brand product.


Q: Does Metrocreme treat acne or is it only for rosacea?

A: Official regulatory documents explicitly indicate that Metrocreme is approved for the topical treatment of the inflammatory papules and pustules of rosacea. The drug is approved for the topical treatment of the inflammatory papules and pustules of rosacea.


Q: How quickly should I expect to see any difference when using Metrocreme?

A: Clinical trials for metronidazole topical have generally assessed symptom changes over periods between 7 and 12 weeks. Some evidence suggests that initial improvement may be noticeable after approximately three weeks of consistent application.


Q: Can Metrocreme interact with over-the-counter facial cleansers or makeup?

A: Official instructions require the skin area to be cleansed with a mild wash before application, and state that patients may apply cosmetics after the cream has fully absorbed. No specific systemic interactions are listed for non-medicated cleansers or makeup.


Q: Is Metrocreme safe to use during pregnancy? (Descriptive inquiry)

A: Metronidazole topical cream is classified as Pregnancy Category B. Official documentation states that it should be used during pregnancy only if clearly needed, noting that the drug does cross the placental barrier.


Q: Do I need to avoid sun exposure while using Metrocreme?

A: While the U.S. label does not explicitly list photosensitivity, general medical guidance often advises minimizing or avoiding strong sunlight exposure for the treated area.


Q: Is a prescription always required for Metrocreme?

A: Metrocreme and its generic equivalents are labeled 'Rx only' by the U.S. Food and Drug Administration (FDA). This classification means a prescription from a licensed healthcare provider is always required for its use.


Q: How does Metrocreme differ from oral medications for rosacea?

A: Metrocreme is a topical medicine applied directly to the skin, resulting in very low systemic absorption, meaning little drug enters the bloodstream. Oral forms of metronidazole result in significantly higher blood levels.


Q: Does the cream concentration (e.g., 0.75% or 1%) affect how it is used?

A: The 0.75% cream formulation is typically directed for twice-daily application. In contrast, certain 1% cream or gel formulations of metronidazole are often labeled for once-daily use, indicating differences in frequency of use by concentration.


Q: Is Metrocreme used for any other skin conditions besides rosacea?

A: Official regulatory indications for Metrocreme strictly list the treatment of inflammatory lesions of rosacea. Other formulations of the active ingredient metronidazole are approved for other conditions, but not this specific topical cream.


Q: What are the most commonly reported side effects of Metrocreme?

A: The most frequently reported adverse reactions, classified as Very Common (affecting 10% or more of patients), include localized symptoms such as skin dryness, scaling, itching (pruritus), and stinging at the application site.


Q: Can certain foods or drinks make Metrocreme less effective?

A: Official labeling advises against the use of alcohol-containing products during therapy and for a period after the last dose. This is due to the potential risk of a disulfiram-like reaction.


Q: Does using Metrocreme mean I don't need to use sunscreen?

A: Official guidance often recommends minimizing or avoiding strong sunlight exposure for the treated area. This generally indicates that continued use of sun protection remains necessary.


Q: Does Metrocreme contain any steroids?

A: The active ingredient in Metrocreme is metronidazole. The official description classifies it as a nitroimidazole antimicrobial agent, and the regulatory documentation does not list any corticosteroid (steroid) as an active ingredient.


Q: Can I use Metrocreme if I have very sensitive skin?

A: While the product utilizes an emollient base that can be soothing, common adverse reactions listed in the official label include dryness, stinging, and contact dermatitis. These documented reactions suggest that localized irritation is still possible.


Q: Does Metrocreme require specific storage conditions?

A: The product is required to be stored at a controlled room temperature, typically between 20 C and 25 C (68 F and 77 F). It must also be protected from freezing, excess heat, and moisture to maintain its stability.


Q: Is it possible to have an allergic reaction to Metrocreme?

A: Yes. Official labeling states that the medication is contraindicated (should not be used) in individuals who have a history of hypersensitivity, which is a type of allergic reaction, to metronidazole or any of the other ingredients in the formulation.


Q: Why do some people experience initial worsening when starting Metrocreme?

A: Rosacea condition worsening is officially listed as a Common adverse reaction, meaning it is an observed event. However, the official regulatory text does not provide a specific medical explanation for why this temporary occurrence may happen in some individuals.


Q: Can men use Metrocreme for their rosacea symptoms?

A: Yes. Metrocreme is indicated for rosacea, a condition that affects both men and women. Clinical trials used to support the product's approval have included adult populations without exclusion based on sex.


Q: Is there a difference in how Metrocreme works compared to other topical gels for rosacea?

A: Metrocreme is formulated with an emollient cream base, which distinguishes it from gel or lotion formulations of metronidazole. This difference in base may affect the texture, skin feel, and application but the active ingredient remains the same.


Q: Do different brands of metronidazole cream work the same as Metrocreme?

A: The FDA determines that generic versions of metronidazole topical cream are bioequivalent and therapeutically equivalent to the brand-name product. This means they are expected to work in the same way and have the same clinical effect.


Q: What should I look out for if a side effect seems serious?

A: Official documentation mentions specific serious reactions, such as Peripheral Neuropathy (nerve pain/tingling). Official documentation notes that patients who suspect a serious adverse reaction should report it to their manufacturer or the U.S. FDA, as part of the regulatory safety process.


Q: Can Metrocreme be used on skin areas other than the face?

A: The indication is for rosacea, which primarily affects the face. The approved route is topical application to the affected skin area.


Q: What are the inactive ingredients in Metrocreme?

A: Official labeling lists the inactive ingredients, which include benzyl alcohol, emulsifying wax, glycerin, isopropyl palmitate, purified water, sorbitol solution, and lactic acid/sodium hydroxide to adjust pH. These ingredients make up the emollient cream base.


Q: Will Metrocreme still work if I use a strong moisturizer with it?

A: Official labeling permits the use of cosmetics after application. Based on clinical practice observations, moisturizers are often used to address potential dryness, and it is suggested they be applied after the medication is fully absorbed.


Q: Why is it important to use Metrocreme consistently?

A: The official administration protocol mandates consistency in frequency, requiring twice-daily application to the entire affected area. This consistency is required to ensure the medication is used strictly according to the approved label and to support the intended therapeutic effect over time.


Q: Does Metrocreme help prevent future rosacea flare-ups?

A: The drug is indicated for the treatment of existing inflammatory lesions and is commonly utilized in maintenance studies, suggesting a role in long-term management of the condition. However, the regulatory text does not explicitly use the term 'prevention'.


Q: Is Metrocreme for all types of rosacea?

A: The official indications for Metrocreme strictly specify the treatment of inflammatory papules and pustules of rosacea. This specific type is only one presentation of the overall condition.

How should Metrocreme be stored and disposed of?

Storage and Disposal Requirements for Metrocreme

Metrocreme (metronidazole topical cream, 0.75%) must be stored according to official regulatory specifications to maintain its stability.

Condition Requirement (Official Labeling)
Temperature Store at Controlled Room Temperature, 20 to 25 C (68 to 77 F).
Prohibitions Do not freeze; protect from excess heat and moisture.
Packaging Keep in the original container, tightly closed. Do not use if the seal is punctured.
Child Safety Keep out of reach of children.

For disposal of expired or unused cream, the best option is to use a community drug take-back program. If a program is unavailable, follow federal guidelines by mixing the cream with an undesirable substance (e.g., used coffee grounds) and sealing it in a container before disposal in household trash. This product is not recommended for disposal by flushing.

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

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