Miconazole 1% Tolnaftate 1% Topical Lotion is a liquid or semi-liquid formulation designed for external application to the skin. It provides a smooth and spreadable consistency, offering therapeutic effects for specific skin conditions.

Licensed to fill prescriptions for patients in RI, MA, CT, NJ, NH, FL, ME and PA. New York patients are served on a limited basis while nonresident registration is pending.
This topical lotion combines Miconazole 1% and Tolnaftate 1%, creating a synergistic antifungal formulation designed for external application to the skin.
Miconazole is an imidazole antifungal agent that works by inhibiting the synthesis of ergosterol, an essential component of fungal cell membranes. This disruption leads to increased membrane permeability and ultimately results in fungal cell death.
Tolnaftate is a synthetic
Miconazole 1% Tolnaftate 1% Topical Lotion is a compounded formulation designed for the treatment of various fungal skin infections, such as athlete's foot, jock itch, and ringworm. This formulation combines the antifungal properties of miconazole and tolnaftate, providing a broad-spectrum approach to combatting dermatophytes and other susceptible fungi. While this topical lotion is generally well-tolerated, it is important to be aware of potential drug interactions that may affect its efficacy or increase the risk of adverse effects.
For patients using this topical lotion, it is crucial to inform healthcare providers of all medications currently being used, including prescription drugs, over-the-counter medications, and herbal supplements. Although systemic absorption of miconazole and tolnaftate from topical application is minimal, there is still a potential for interactions, particularly with medications that are metabolized by the cytochrome P450 enzyme system. Miconazole, in particular, is known to inhibit CYP3A4, an enzyme responsible for the metabolism of many drugs. This inhibition can lead to increased plasma concentrations of drugs metabolized by CYP3A4, potentially resulting in enhanced effects or toxicity.
Patients using oral anticoagulants, such as warfarin, should exercise caution, as miconazole may potentiate the effects of these medications, increasing the risk of bleeding. Regular monitoring of INR levels is recommended for patients on anticoagulant therapy who are also using this topical formulation. Additionally, patients taking oral hypoglycemic agents or insulin should be aware that miconazole may enhance the hypoglycemic effects, necessitating close monitoring of blood glucose levels to prevent hypoglycemia.
For prescribers, it is important to consider the patient's complete medication profile before recommending Miconazole 1% Tolnaftate 1% Topical Lotion. Assessing the potential for drug interactions, especially with medications that have a narrow therapeutic index, is essential to ensure patient safety. In cases where significant interactions are identified, alternative treatments or additional monitoring may be necessary.
Patients should be advised to apply the lotion as directed, typically to clean, dry skin, and to avoid occlusive dressings unless specifically instructed by a healthcare provider. It is also important to counsel patients on the signs of potential adverse reactions, such as skin irritation or allergic reactions, and to seek medical advice if these occur.
If you have any questions or concerns regarding the use of Miconazole 1% Tolnaftate 1% Topical Lotion, or if you need further information on potential drug interactions, please reach out to us at Bayview Pharmacy. Our team of knowledgeable compounding pharmacists is here to assist you with any inquiries you may have.
This formulation combines two potent antifungal agents, miconazole and tolnaftate, each contributing unique mechanisms of action to combat dermatophytes, yeasts, and molds that cause skin infections. Miconazole, an imidazole antifungal, works by inhibiting the synthesis of ergosterol, a critical component of fungal cell membranes. By disrupting the production of ergosterol, miconazole compromises the integrity of the fungal cell membrane, leading to cell death and resolution of the infection.
Tolnaftate, on the other hand, is a thiocarbamate antifungal that interferes with the fungal life cycle by inhibiting squalene epoxidase, an enzyme essential for ergosterol synthesis. This inhibition results in the accumulation of squalene, which is toxic to fungal cells, and further disrupts the cell membrane, enhancing the antifungal effect. The combination of these two active ingredients in a single formulation provides a broad-spectrum approach to treating fungal infections.
The topical lotion is designed to be applied externally to the affected areas of the skin. Its liquid or semi-liquid consistency ensures ease of application, allowing for a smooth and even distribution over the skin surface. This formulation not only delivers the active ingredients directly to the site of infection but also promotes their absorption into the skin, enhancing their therapeutic effects. The lotion base may also contain moisturizing and soothing agents that help to alleviate symptoms such as itching, redness, and irritation, providing additional comfort to the patient during the treatment process.
The dual-action of miconazole and tolnaftate provides a comprehensive approach to treatment, reducing the likelihood of resistance development and improving patient outcomes. Patients are advised to apply the lotion as directed, typically once or twice daily, and to continue treatment for the full duration prescribed, even if symptoms improve, to ensure complete eradication of the infection.
If you have any questions about this formulation or its use, please do not hesitate to reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is here to provide you with the information and support you need to achieve the best possible outcomes for your patients.
This topical lotion is used to treat fungal skin infections such as athlete's foot, jock itch, and ringworm. It combines the antifungal properties of Miconazole and Tolnaftate to effectively target and eliminate fungal growth.
Apply a thin layer of the lotion to the affected area and surrounding skin once or twice daily, or as directed by your healthcare provider. Ensure the skin is clean and dry before application.
While this lotion is designed for external use, it is important to avoid contact with the eyes, mouth, and other mucous membranes. Consult your healthcare provider before using it on sensitive areas like the face.
Improvement in symptoms can typically be seen within a few days of consistent use. However, it is important to complete the full course of treatment as prescribed to ensure the infection is fully cleared.
Some users may experience mild skin irritation, redness, or itching at the application site. If these symptoms persist or worsen, discontinue use and consult your healthcare provider.
If you are pregnant or breastfeeding, consult your healthcare provider before using this lotion to ensure it is safe for you and your baby.
Consult a healthcare provider before using this lotion on children, as they can provide guidance based on the child's specific condition and age.
It is generally safe to use other skincare products; however, avoid applying them directly on top of the medicated lotion to ensure proper absorption of the active ingredients. Consult your healthcare provider for personalized advice.
If you miss a dose, apply it as soon as you remember. If it is almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose to catch up.
Store the lotion at room temperature, away from direct sunlight and moisture. Keep it out of reach of children and pets to prevent accidental ingestion or misuse.
This formulation is compounded by Bayview Pharmacy on a prescriber's order for an individual patient. It is not an FDA-approved drug product, and the FDA has not evaluated it for safety, effectiveness, or manufacturing quality.
A valid prescription is required. Availability depends on Bayview's licensure in your state. This page is general information, not medical advice. Discuss your situation with a licensed healthcare provider.
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Compounded preparations have no NDC, so this formula will not appear in your EHR's drug search. Use your system's compound, non-formulary, or free-text prescription entry and name the preparation exactly as written in step 3. If your EHR forces you to pick a listed drug, pick the closest entry for the active ingredient and put the full formula in the prescription body (the Sig or directions field), not in Notes to Pharmacy.
Compounded preparations have no NDC and will not appear in your drug search. For EPCS to validate, select a drug entry your EHR recognizes as controlled, usually the bulk powder entry for the active ingredient (for example Ketamine (bulk) powder, not a branded product), then put the full formula from step 3 in the prescription body. A free-text entry that does not validate as controlled will be rejected by your EPCS module.
Quantity and directions are starting points for this dose form, not treatment recommendations. Dosing remains the prescriber's responsibility.
Transmit from your EHR. For this non-controlled preparation we also accept fax to (401) 284-4506 and phoned orders at (401) 284-4505. Order forms are on the formulation pages and in the prescriber portal.
Transmit with two-factor authentication through your EPCS-enabled EHR. No order form is offered for this preparation; e-prescribing guides for our controlled preparations are on the formulation pages.
Licensed to dispense in RI, MA, CT, NJ, NH, FL, ME, and PA; New York is served on a limited basis while nonresident registration is pending. Compounded preparations are not FDA-approved. A valid prescription is required. Full guide, including steps by EHR: How to e-prescribe to Bayview. Questions about this formula: call (401) 284-4505.
Apply topically to affected area(s)