Dermatin 1%

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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 Dermatin 1%

Quick Facts

Property Description
Active Ingredient Clotrimazol (Clotrimazole)
Form Topical Cream, Topical Solution
Pharmacological Class Imidazole Antifungal Agent
Route of Administration Dermal (Topical)
Origin Synthetic Organic Compound

What Type of Medication is Dermatin 1%? (Definition, Class, and Composition)

Dermatin 1% is a topical preparation that contains the active antifungal ingredient Clotrimazol (Clotrimazole), a compound chemically identified as an imidazole derivative. This medication is categorized within the pharmacological class of Azole Antifungals or Antimycotic Agents. Clotrimazol is a synthetic organic compound, which distinguishes it from historically used botanically derived treatments. As a single-ingredient preparation specifically designed for the dermal route of administration, Dermatin 1% is used to treat localized mycotic outbreaks, often targeting adults and certain pediatric groups. The designation "1% concentration" signifies that the product contains ten milligrams of Clotrimazol for every gram or milliliter of the inert base, available as either a cream or a solution.

The General Purpose of Clotrimazol (Mechanism-Free Benefit)

The fundamental general purpose of Dermatin 1% is to serve as a focused antimycotic agent to combat and help eliminate the fungal organisms responsible for superficial skin infections. Clotrimazol is utilized for its broad-spectrum capability, meaning it is effective against a wide variety of pathogenic yeasts and dermatophytes. This preparation's mechanism involves causing structural damage to the fungal cell membrane, which leads to the cessation of growth and reproduction of the organism. The core therapeutic benefit is focused on arresting the underlying mycotic proliferation to help restore the affected area of the skin to its healthy state, without addressing symptoms like inflammation or pain, which require separate agents.

Regulatory References

  1. WHO Essential Medicines List for Clotrimazole
  2. Clotrimazole Mechanism of Action (NCBI/NIH)

What side effects are possible with Dermatin 1%?

Possible Side Effects and Safety Information

Dermatin 1% (clotrimazole topical cream) has a safety profile that is primarily characterized by effects localized to the application site. Regulatory documents describe both common local reactions and the potential for rare, serious systemic events.

Adverse Reactions and Safety Restrictions

Adverse reactions reported in official sources generally fall under the System-Organ Class of Skin and Subcutaneous Tissue Disorders. These are typically reactions of local irritation and may include:

  • Burning, stinging, or pain
  • Redness or erythema
  • Itching (pruritus)
  • Swelling or blistering
  • Peeling

The documentation emphasizes that use must be discontinued and a healthcare provider consulted if irritation, swelling, blistering, or other signs of skin irritation not present before use occur. These local reactions define the most common safety events associated with this topical medicine.

Serious Adverse Reactions

Although rare, clotrimazole preparations carry a documented risk of Systemic Allergic Reactions or Hypersensitivity Reactions. Symptoms associated with a serious allergic reaction may include swelling of the face, lips, tongue, or throat, or difficulty swallowing or breathing. These symptoms require immediate medical attention.

Population-Specific Safety Considerations

The official safety information for this product includes a specific restriction regarding the pediatric population:

  • Use in children under two years of age is restricted and must not occur without the direction of a healthcare provider.

Furthermore, the regulatory guidance strictly advises that this product is for external use only and must be kept out of the eyes. If the product is swallowed, emergency medical help or a Poison Control Center must be contacted immediately.

Overdose and Emergency Response

Overdose and when to seek help

The official regulatory profile for Dermatin 1% (Clotrimazole Topical) indicates that acute systemic overdose is unlikely following its dermal application. This is because the active ingredient, Clotrimazole, exhibits minimal systemic absorption through the skin, a finding consistent across governmental prescribing information.


Overdose Scope and Manifestations

The primary overdose concern is associated with the accidental oral ingestion of the cream or solution. Regulatory documents confirm that if the product is swallowed, the documented manifestations may include gastrointestinal distress, such as nausea and vomiting. Systemic toxicity from routine topical use is generally not predicted. No specific antidote is known, and no unique population-specific overdose considerations are detailed in official labeling.


Emergency Response and Management

The most critical regulatory instruction is to seek immediate medical attention and contact a Poison Control Center if any accidental ingestion occurs. This action is mandated due to the ingestion hazard. Official prescribing information states that treatment must consist of symptomatic and supportive measures. Monitoring may be required based on the extent of the oral ingestion.


Official Statement Summary

The regulatory framework defines this product's overdose risk primarily by the ingestion route and mandates urgent medical consultation for accidental swallowing, while acknowledging the low likelihood of acute systemic effects from topical application. Treatment is limited to supportive care.

Therapeutic Uses of Dermatin 1%

What Dermatin 1% Treats: Main Uses and Benefits

Dermatin 1% is commonly used in addressing common superficial skin infections caused by yeasts and dermatophytes. Its core purpose is generally to help address relevant fungal issues and provide symptomatic relief for associated discomfort. This therapeutic domain includes the management of infections such as Tinea pedis (Athlete's foot), Tinea cruris (Jock itch), Tinea corporis (Ringworm), and other forms of Cutaneous Candidiasis.


The medication is used for managing the fungal pathogen, which generally supports the improvement of the condition and contributes to supporting skin health. It is commonly applied in situations involving pronounced pruritus (intense itching) and a painful burning sensation that are characteristic of active fungal infections. The application is relevant for providing supportive relief during symptomatic periods. The application is also relevant for managing the physical damage caused by the infection, such as scaling, peeling, and painful cracking of the skin surface, especially in warm, moist areas, and may assist with maintaining comfort and stability.


Quick Fact: Relevant for Pruritus and Burning (The medication may assist with easing the overall symptom burden of intense itching and irritation.)

Regulatory References

  1. NIH DailyMed Drug Facts on Clotrimazole Topical

Eligibility and Restrictions for Use

Dermatin 1%, which contains the antifungal medication clotrimazole, is an external topical cream generally used to treat common fungal skin infections such as athlete's foot, jock itch, and ringworm in most adults and children.


Individuals Who May Use Dermatin 1%

Category Conditions of Use
Adults Treatment of tinea (ringworm, athlete's foot, jock itch) and candidiasis of the skin.
Children 2 Years and Older Generally considered safe for use. Supervision of application for children under 12 years of age is often recommended.
Elderly No specific age-related precautions are generally required for topical use.

Individuals Who Should Not Use Dermatin 1% or Consult a Doctor

Contraindication/Caution Rationale
Known Allergy Individuals with a documented hypersensitivity to clotrimazole or any other ingredient in the cream.
Children Under 2 Years Old Should not be used unless specifically directed and supervised by a healthcare provider.
Application to Eyes/Mouth This medication is for external skin use only and should be kept away from the eyes and mucous membranes.
No Improvement If symptoms do not improve within a specified period (e.g., four weeks for athlete's foot/ringworm, two weeks for jock itch), consult a doctor.
Pregnancy/Breastfeeding Consultation with a healthcare provider is recommended to weigh the potential benefits against any risks.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Official regulatory documentation details the specific interaction patterns and use restrictions for Dermatin 1% (Clotrimazole topical cream/solution). The primary constraints relate to product-substance integrity and potential pharmacodynamic or pharmacokinetic alterations.

Interaction Type (High-Level) Interacting Substances / Products Official Regulatory Constraint
Product Integrity Restriction Latex Contraceptives (condoms, diaphragms) Co-application to the genital area reduces the efficacy and safety of the device due to physical damage to the latex.
Timing-Based Rule Latex Contraceptives Alternative precautions must be maintained for at least five days following the product's application to the genital area.
Pharmacodynamic Antagonism Polyene Antibiotics (e.g., Nystatin, Amphotericin B) Co-administration with certain other topical antifungal agents may reduce the intended antifungal effect on the skin surface.
Systemic Exposure Alteration Oral Tacrolimus and Oral Sirolimus Potential for increased plasma concentrations of these agents due to inhibition of metabolic enzymes, though this risk is unlikely to be clinically relevant with the minimal systemic absorption from dermal use.

Regulatory documentation also notes that there are no known interactions between the topical formulation and foods or drinks. The official interaction profile is structured around these specific restrictions and documented potential for reduced efficacy or heightened systemic drug levels, providing the necessary boundaries for co-use.

Mechanism of Action

Targeting the Fungal Cell's Structural Building Blocks

Dermatin 1% (Clotrimazole) works by engaging the key enzyme lanosterol 14-alpha-demethylase (CYP51) found in fungal cells, acting as an inhibitor to block its function. This action prevents the fungus from synthesizing ergosterol, the vital lipid required to build and maintain its cell membrane . This mechanism is unique to the fungal pathway and does not directly target human cholesterol synthesis.


Compromising Membrane Integrity and Fungal Viability

The blockade of ergosterol production causes abnormal lipid precursors to accumulate, which destabilizes the fungal cell membrane, resulting in abnormal permeability and failure of structural integrity. This physical compromise results in the leakage of essential cellular contents and the failure of processes like cell division and growth. This cascade ultimately leads to the biological suppression of the fungal population, consistent with the mechanistic consequence of membrane failure.

Dosage and Administration Information

Dermatin 1% (clotrimazole topical) is an antifungal medication indicated for treating dermal infections such as athlete's foot, jock itch, and ringworm. The cream is for external use only and should be applied strictly as directed on the product label or by a physician.

Application Guidelines

  1. Preparation: Prior to application, the affected area of the skin must be thoroughly washed and dried.
  2. Dosage: Gently apply a thin layer of the 1% cream over the entire affected area and the surrounding skin.
  3. Frequency: The medication is typically applied twice daily, generally in the morning and evening, or as advised by a healthcare professional.

Duration of Treatment

It is crucial to use the medication for the full recommended treatment duration, even if symptoms begin to clear, to help prevent the infection from returning. The general duration varies by condition:

Condition Treatment Duration (Daily Use)
Jock Itch 2 weeks
Athlete's Foot or Ringworm 4 weeks

If the condition shows no clinical improvement after the specified treatment time, or if the symptoms worsen, consult a doctor to re-evaluate the diagnosis.

Special Considerations:

  • For treating athlete's foot, pay particular attention to the spaces between the toes, ensure footwear is well-ventilated, and change socks daily.
  • Avoid contact with the eyes. Do not use this product on the scalp or nails, as it is generally ineffective for those areas.
  • Stop use and consult a healthcare professional if irritation or a sensitivity reaction occurs.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Dermatin 1%


Evidence for Use in Dermatophyte Infections (Athlete’s Foot, Ringworm, Jock Itch)

The research base for Dermatin 1% in common fungal skin infections, such as Athlete's foot (Tinea pedis) and Ringworm (Tinea corporis), largely consists of Randomized Controlled Trials (RCTs) and controlled clinical studies. These trials were designed to observe differences between the topical medicine and an inactive cream or solution (vehicle).

Researchers in these studies primarily examined two types of outcomes: mycological endpoints (laboratory checks to monitor the fungal organism's status) and clinical endpoints (patient-reported changes in symptoms like skin scaling, redness, and itching). The evidence landscape from these studies suggests patterns related to mycological outcomes and describes the evolution of physical symptoms during the short-term study period. The evidence for managing recurrent, chronic, or highly treatment-resistant forms of these infections remains less extensive.


Evidence for Use in Cutaneous Yeast Infections (Candidiasis and Tinea Versicolor)

For skin conditions caused by yeasts, such as Cutaneous Candidiasis and Tinea Versicolor, the evidence base also relies on Randomized Controlled Trials (RCTs). These studies were intended to explore how the 1% clotrimazol preparation compared against its inactive base. Research focused on the laboratory-confirmed status of Candida species and the Malassezia fungus.

The studies reported measurements of both mycological clearance and the clinical resolution of visible skin lesions and irritation after short treatment courses, often lasting only one to two weeks. Findings indicated consistent patterns in the measured outcomes related to mycological outcomes measured over the short study duration. Research for outcomes involving less common fungal strains or in patients with compromised immune systems is not widely available in the current body of research.


What is Still Uncertain about Dermatin 1% (Research Gaps)

The available research highlights several areas where further information is needed:

  • Long-term Outcomes: There is limited information for long-term outcomes, especially regarding the rate and timing of infection recurrence beyond a few months of observation.
  • Subgroup Findings: Data for certain groups remain insufficient, particularly for immunocompromised individuals or those dealing with chronic or complex infections.
  • Consistency of Measures: Evidence quality varies across some studies, particularly due to differences in how specific clinical symptoms were measured and defined in older trials. Research helps show what has been observed so far in group patterns, but research does not determine whether an individual will respond similarly.

Key Studies & References

  1. Clotrimazole - StatPearls (Review covering pharmacology, indications, and general trial design)
  2. FDA Label: CLOTRIMAZOLE 1%- clotrimazole cream (Includes indications, warnings, and pediatric use information)
  3. PRODUCT MONOGRAPH CLOTRIMADERM Clotrimazole (Topical Cream 1%) Antifungal Agent (Includes special populations and stability)

Frequently Asked Questions (FAQ)

Common questions about Dermatin 1% (FAQ)

Q: What happens if I forget a dose?

A: According to official product information, if a dose is remembered soon after it was missed, instructions state to apply the cream. However, if it is close to the time for the next scheduled application, the missed dose is typically skipped, and the regular schedule is continued. Official information advises against using a double amount to compensate for a missed dose.


Q: What happens if my skin gets worse or I have a bad reaction to the cream?

A: If the condition does not improve after the specified treatment duration, or if the area of application shows new or increased irritation, official guidance is to discontinue use of the product. The product label recommends notifying a healthcare professional if signs of severe irritation, such as blistering, increased redness, swelling, burning, or oozing, occur.


Q: How does this drug actually kill the fungus?

A: Studies and official information indicate that the active ingredient, clotrimazole, works by causing damage to the fungal cell membrane, which is vital for the fungus's ability to grow and survive. This action is consistent with the process that leads to the biological suppression of the fungal population and helps resolve the infection.


Q: Does this cream help with the itching?

A: Official data indicates that relief of itching (pruritus) and irritation associated with the fungal infection is part of the expected clinical improvement. This outcome is generally observed within the first week of treatment.


Q: Is this cream safe to use for babies under 2 years old?

A: The official regulatory guidance states that Dermatin 1% is restricted from use in children under 2 years of age. Consultation with a healthcare provider is required before use in this age group, according to regulatory guidance.

How should Dermatin 1% be stored and disposed of?

Official Storage and Disposal Requirements

Condition Requirement
Temperature Store at controlled room temperature, typically between 20 C and 25 C (68 F and 77 F).
Protection Keep from freezing, excessive heat, moisture, and direct light.
Container Must be kept in a closed container and out of the reach of children.

This medicine must be stored under controlled conditions to maintain stability, specifically avoiding freezing, which is a prohibited environment. Official regulatory guidelines strictly require that the product be kept out of the sight and reach of children. Unused or expired Dermatin 1% should be disposed of properly according to local regulations; it must not be flushed down the toilet or poured down any drain. The FDA advises mixing it with an undesirable substance, sealing it in a separate container, and placing it in household trash if a medicine take-back program is unavailable.

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

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