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Bayview Pharmacy's Clindamycin 1%/Lidocaine 1%/Naltrexone HCl 1%/Clobetasol Propionate 0.05% Topical Gel is a specially compounded medication. This semisolid formulation is dispensed through a pump mechanism, allowing for easy and precise application on the skin. It is designed for targeted treatment or absorption of active ingredients in a gel-like consistency. It is used to treat conditions such as Atopic Dermatitis, Psoriasis, Seborrheic Dermatitis, Lichen Planus, and Acne Vulgaris.
Licensed to fill prescriptions for patients in RI, MA, CT, NY, NJ, NH, FL and ME.
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Bayview Pharmacy is pleased to present a specialized topical gel formulation of Clindamycin 1%/Lidocaine 1%/Naltrexone HCl 1%/Clobetasol Propionate 0.05%. This unique compound is specifically designed to address a range of skin conditions such as acne, eczema, psoriasis, and contact dermatitis. The blend of active ingredients offers anti-inflammatory, anti-bacterial, and analgesic properties, making it a potent treatment for these skin conditions.
Clindamycin, an antibiotic in the formulation, works to decrease the number of bacteria on the skin. Lidocaine, an anesthetic, aids in reducing pain and itching associated with skin conditions. Naltrexone HCl, an opioid antagonist, contributes to the reduction of inflammation. Lastly, Clobetasol Propionate, a corticosteroid, further assists in reducing inflammation and itching.
This compounded formulation is dispensed through a pump mechanism, facilitating easy and precise application on the skin for targeted treatment or absorption of active ingredients in a gel-like consistency. This ensures that the medication is applied exactly where it's needed, enhancing its effectiveness while minimizing potential side effects.
It's important to contact your healthcare provider if you experience any adverse reactions or have any concerns.
If you have any questions about this formulation or how it can be used to treat your specific skin condition, please don't hesitate to contact us at Bayview Pharmacy. Our team is here to assist you in finding the most suitable treatment for your skin condition.
This compounded formulation of Clindamycin 1%/Lidocaine 1%/Naltrexone HCl 1%/Clobetasol Propionate 0.05% is a semisolid topical gel designed for targeted treatment of various skin conditions. It is dispensed through a pump mechanism, which allows for easy and precise application on the skin. The gel-like consistency aids in the absorption of the active ingredients.
The formulation is indicated for the treatment of acne, psoriasis, eczema, and dermatitis, as well as the itching, burning, and pain associated with these conditions. The combination of Clindamycin and Lidocaine works to reduce inflammation and provide relief from pain and itching. Naltrexone HCl is included to help reduce the severity of the skin condition, while Clobetasol Propionate works to reduce redness and swelling.
Patients are advised to apply a thin layer of the topical gel to the affected area twice daily, or as directed by their healthcare provider. It is important to avoid contact with the eyes, nose, and mouth. If contact occurs, the area should be rinsed with water. This product should not be used for longer than two weeks unless directed by a healthcare provider.
Patients should immediately contact their healthcare provider if they experience any signs of an allergic reaction, such as hives, difficulty breathing, or swelling of the face, lips, tongue, or throat. Signs of infection, such as redness, swelling, or pus, should also be reported to a healthcare provider.
Prescribers are advised to use caution when prescribing this product to patients with a history of hypersensitivity to any of the ingredients. Additionally, caution should be used when prescribing this product to patients with a history of liver or kidney disease, as the combination of ingredients may increase the risk of adverse effects.
If you have any questions about this formulation or how it interacts with other medications, please consult with your healthcare provider or pharmacist.
Clindamycin 1%/Lidocaine 1%/Naltrexone HCl 1%/Clobetasol Propionate 0.05% Topical Gel is a compounded formulation that combines four potent active ingredients, each with a unique role in treating various skin conditions. This semisolid formulation is dispensed through a pump mechanism, ensuring easy and precise application on the skin.
Clindamycin, an antibiotic, works by reducing the number of bacteria on the skin, thereby preventing or treating bacterial infections. Lidocaine, a local anesthetic, provides relief from pain and discomfort associated with certain skin conditions. Naltrexone HCl, an opioid antagonist, aids in reducing inflammation and itching, while Clobetasol Propionate, a corticosteroid, helps to alleviate redness and swelling.
This combination of ingredients is designed to effectively manage symptoms of various skin conditions, including acne, eczema, psoriasis, and rosacea. The gel-like consistency of the formulation allows for targeted treatment or absorption of these active ingredients, providing relief right where it's needed.
To use this topical gel, apply a thin layer to the affected skin area twice daily, gently massaging until it is fully absorbed. It is important to avoid applying the gel to broken or irritated skin, and to avoid contact with the eyes and mouth. If any irritation or discomfort occurs, discontinue use and consult with your healthcare provider immediately.
If you have any questions or concerns about Clindamycin 1%/Lidocaine 1%/Naltrexone HCl 1%/Clobetasol Propionate 0.05% Topical Gel, or if you need further information on how it can help manage your skin condition, please do not hesitate to reach out to us. We are committed to helping you find the most suitable treatment for your needs.
This compounded formulation of Clindamycin 1%/Lidocaine 1%/Naltrexone HCl 1%/Clobetasol Propionate 0.05% is a semisolid topical gel designed for precise application on the skin. It is dispensed through a pump mechanism, which facilitates easy and accurate application, ensuring the targeted treatment or absorption of the active ingredients. This formulation is primarily used for the treatment of various skin conditions including Atopic Dermatitis, Psoriasis, Seborrheic Dermatitis, Lichen Planus, and Acne Vulgaris. It can also be beneficial in managing other skin conditions such as contact dermatitis, eczema, and pruritus.
The combination of Clindamycin and Lidocaine in the formulation works to alleviate inflammation and itching associated with these conditions. Simultaneously, Naltrexone HCl and Clobetasol Propionate work together to reduce redness and swelling, providing relief from discomfort. This topical gel should be applied directly to the affected area as directed by your healthcare provider. It is crucial to adhere to the instructions provided on the label and avoid contact with sensitive areas such as the eyes, nose, and mouth.
If you have any questions or concerns regarding the use of this formulation, please do not hesitate to reach out to us at Bayview Pharmacy.
This compounded formulation is designed to deliver multiple active ingredients directly to the skin for targeted treatment. It contains Clindamycin, Lidocaine, Naltrexone HCl, and Clobetasol Propionate, each serving a unique therapeutic purpose.
This gel is dispensed through a pump mechanism for easy and precise application. Apply it to the affected area as directed by your healthcare provider, usually in a thin layer.
This formulation is a semisolid, gel-like consistency. It is designed to be easily spreadable and quickly absorbed by the skin.
The active ingredients in this formulation are Clindamycin 1%, Lidocaine 1%, Naltrexone HCl 1%, and Clobetasol Propionate 0.05%.
Clindamycin is an antibiotic that fights bacteria, Lidocaine is a local anesthetic, Naltrexone HCl is used to manage addiction, and Clobetasol Propionate is a corticosteroid that reduces inflammation.
This formulation is intended for topical use only. Avoid contact with eyes, mouth, and other mucous membranes. Always use it as directed by your healthcare provider.
If you experience any side effects such as redness, irritation, or swelling at the application site, stop using the product and contact your healthcare provider immediately.
Store this formulation at room temperature, away from heat and direct light. Do not freeze. Keep out of the reach of children and pets.
If you are pregnant or breastfeeding, consult your healthcare provider before using this formulation. Some ingredients may be absorbed into the bloodstream and could potentially affect the baby.
If you miss a dose, apply it as soon as you remember. However, 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 double the dose to catch up.
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, NY, NJ, NH, FL, and ME. 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)
