Bayview Pharmacy's Ketoconazole 2%/Betamethasone Valerate 0.1%/Zinc Pyrithione 0.2% Topical Gel is a semisolid formulation dispensed through a pump mechanism. This allows for easy and precise application on the skin, facilitating targeted treatment of various skin conditions. These include Seborrheic Dermatitis, Tinea Versicolor, Psoriasis, Atopic Dermatitis, and Acne Vulgaris.

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.
Bayview Pharmacy is pleased to present a specialized topical gel formulation of Ketoconazole 2%, Betamethasone Valerate 0.1%, and Zinc Pyrithione 0.2%. This unique compound is specifically designed to address a range of skin conditions such as seborrheic dermatitis, psoriasis, and atopic dermatitis.
Ketoconazole, an antifungal agent, works to alleviate inflammation and itching commonly associated with these skin conditions. Betamethasone Valerate, a corticosteroid, further aids in reducing inflammation and itching. Zinc Pyrithione is included in the formulation for its ability to minimize scaling and flaking.
This semisolid formulation is dispensed through a pump mechanism, facilitating easy and precise application on the skin for targeted treatment. The gel-like consistency allows for optimal absorption of the active ingredients. Depending on the severity of the skin condition, this formulation can be applied once or twice daily.
It is crucial to note that this formulation should not be used on the face, groin, or axillae, and its usage should not exceed a duration of two weeks. If you have any queries about this formulation or its application, please do not hesitate to contact us at Bayview Pharmacy.
Ketoconazole 2%/Betamethasone Valerate 0.1%/Zinc Pyrithione 0.2% Topical Gel is a compounded formulation specifically designed for the treatment of various inflammatory skin conditions such as seborrheic dermatitis and psoriasis. This semisolid formulation is dispensed through a pump mechanism, which allows for easy and precise application on the skin, ensuring targeted treatment and optimal absorption of the active ingredients.
The combination of Ketoconazole, Betamethasone Valerate, and Zinc Pyrithione in this formulation works synergistically to reduce inflammation, itching, and scaling associated with these skin conditions. Ketoconazole is an antifungal medication that prevents the growth of fungus, Betamethasone Valerate is a potent corticosteroid that reduces swelling, itching, and redness, and Zinc Pyrithione is an antibacterial and antifungal agent that helps to treat and prevent skin conditions.
It is crucial to note that this formulation should not be applied on the face, groin, or axillae to avoid potential irritation. It is also contraindicated in patients with known hypersensitivity to any of the components. Patients should be advised to avoid contact with the eyes and to wash their hands immediately after application. The use of this product should be limited to the shortest duration necessary to achieve the desired therapeutic effect. In case of any adverse reactions, patients should immediately discontinue use and consult their healthcare provider.
Ketoconazole 2%/Betamethasone Valerate 0.1%/Zinc Pyrithione 0.2% Topical Gel is a compounded medication designed to address various skin conditions such as seborrheic dermatitis, psoriasis, and eczema. This unique formulation combines the antifungal properties of Ketoconazole, the anti-inflammatory and itch-relieving effects of Betamethasone Valerate, and the antiseptic and descaling benefits of Zinc Pyrithione. Together, these active ingredients work synergistically to alleviate symptoms and promote healthier skin.
The gel is dispensed through a pump mechanism, which allows for easy and precise application. This ensures that the medication is delivered directly to the affected area, enhancing its effectiveness. It is recommended to apply this topical gel to the affected skin area once or twice daily, or as instructed by your healthcare provider. Always remember to wash your hands before and after application to prevent the spread of infection.
It is crucial to avoid contact with the eyes, nose, and mouth when applying this medication. In case of accidental contact, rinse the area thoroughly with water. Unless advised by your healthcare provider, do not cover the treated area with a bandage or any other type of covering, as this could affect the absorption of the medication.
If you have any questions or concerns about using Ketoconazole 2%/Betamethasone Valerate 0.1%/Zinc Pyrithione 0.2% Topical Gel, do not hesitate to reach out. It's important to us that you understand your medication and feel confident in its use. We're here to support you every step of the way.
This compounded formulation of Ketoconazole 2%, Betamethasone Valerate 0.1%, and Zinc Pyrithione 0.2% in a topical gel form is a versatile treatment option for a variety of skin conditions. It is dispensed through a pump mechanism, which allows for easy and precise application on the skin. The gel-like consistency ensures targeted treatment or absorption of the active ingredients.
It may be used to treat conditions such as contact dermatitis, lichen planus, and pityriasis rosea. This formulation may also be beneficial in treating bacterial skin infections, such as impetigo and folliculitis.
However, it is crucial to remember that this formulation should only be used to treat skin conditions that have been diagnosed by a healthcare professional. Self-diagnosis and treatment can lead to complications or worsening of the condition. Always consult with a healthcare professional before starting any new treatment regimen.
This formulation is designed to treat various skin conditions. Ketoconazole is an antifungal that prevents fungus from growing on your skin. Betamethasone Valerate is a potent corticosteroid that reduces itching, redness, and swelling. Zinc Pyrithione is an antibacterial and antifungal agent that treats dandruff and seborrhoeic dermatitis.
Apply a thin layer of the gel to the affected area as directed by your healthcare provider. The pump mechanism allows for easy and precise application.
The gel is a semisolid formulation, which means it has a gel-like consistency that is easy to apply and absorbs well into the skin.
Unless directed by your healthcare provider, it is generally not recommended to use this gel on your face due to the potency of the active ingredients. Always follow your healthcare provider's instructions.
If you experience any side effects such as burning, itching, or irritation at the application site, contact your healthcare provider immediately.
Consult your healthcare provider before using this gel if you are pregnant or breastfeeding. They will be able to advise you based on your specific situation.
Store this gel at room temperature, away from heat and direct light. Do not freeze. Keep out of the reach of children.
If you miss a dose, apply it as soon as you remember. If it is close to the time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not apply extra to make up for a missed dose.
Before using other skincare products, consult with your healthcare provider to avoid any potential interactions or adverse effects.
If you think there has been an overdose, call your poison control center or get medical care right away. Be ready to tell or show what was taken, how much, and when it happened.
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.
The conditions listed on this page are indications prescribers have ordered this preparation for. They are not FDA-approved indications, and listing them is not a statement that this preparation is effective for them.
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)