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Naltrexone HCl 0.1% Topical Cream is a compounded formulation designed for localized treatment of skin conditions such as Atopic Dermatitis, Psoriasis, Acne, Rosacea, and Eczema. This semisolid preparation is dispensed via a pump mechanism for convenient and controlled application directly on the affected area.
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.
Naltrexone HCl 0.1% Topical Cream is a specially compounded medication designed to address various skin conditions. This unique formulation combines naltrexone hydrochloride, a synthetic opioid antagonist, with a cream base to create a topical treatment. It is primarily used to manage skin conditions such as psoriasis, eczema, and dermatitis.
The mechanism of action of Naltrexone HCl 0.1% Topical Cream involves the blocking of opioid receptors in the skin. This action helps to alleviate inflammation and itching. Additionally, the cream aids in reducing the production of inflammatory cytokines, which further contributes to the reduction of inflammation and itching. The cream is dispensed in a pump mechanism, which allows for convenient and controlled application on the skin for localized treatment or absorption of the active ingredients.
This formulation is generally well-tolerated by most patients and is easy to apply. As a compounding pharmacy, we are dedicated to creating high-quality, customized medications to cater to the unique needs of our patients.
If you have any queries about Naltrexone HCl 0.1% Topical Cream or any other compounded medications, we encourage you to reach out to us. Our team of compounding pharmacists is equipped with the knowledge and experience to answer your questions and provide the necessary guidance.
Naltrexone HCl 0.1% Topical Cream is a semisolid preparation, specifically formulated for the treatment of skin conditions such as psoriasis, atopic dermatitis, and pruritus. This non-steroidal anti-inflammatory drug (NSAID) functions by inhibiting the production of certain inflammatory substances within the body, thereby alleviating symptoms associated with these conditions.
The cream is designed for topical application, to be applied directly to the affected area twice daily. It is dispensed via a pump mechanism, which allows for a convenient and controlled application. However, it is crucial to avoid using this cream on broken or irritated skin, and to prevent contact with the eyes, nose, and mouth.
Common side effects may include burning, stinging, itching, redness, or dryness at the application site. If any of these side effects occur, it is recommended to contact a healthcare provider immediately. Furthermore, patients should inform their healthcare provider if they are pregnant, breastfeeding, or taking any other medications.
It is important to note that Naltrexone HCl 0.1% Topical Cream may interact with other medications, including certain antibiotics, antifungals, and anticoagulants. Therefore, a comprehensive discussion with a healthcare provider is advised to understand potential interactions and contraindications. If you have any questions or concerns about using Naltrexone HCl 0.1% Topical Cream, please consult with your healthcare provider.
Naltrexone HCl 0.1% Topical Cream is a compounded formulation designed for localized treatment of various skin conditions and opioid addiction. This semisolid preparation is dispensed in a pump mechanism, ensuring a convenient and controlled application on the skin.
For skin conditions such as psoriasis, eczema, and atopic dermatitis, the cream works by blocking the action of certain chemicals in the body that cause inflammation and itching. It is typically applied directly to the affected area of skin, usually twice daily. Overuse or misuse can lead to skin irritation or other side effects, so it is crucial to follow the directions provided by your healthcare professional. It is also important to avoid contact with the eyes, mouth, and other mucous membranes.
In addition to treating skin conditions, Naltrexone HCl 0.1% Topical Cream is also used in the treatment of opioid addiction. It functions by blocking the effects of opioids, such as heroin and prescription pain medications, thereby reducing cravings for these drugs. The cream is usually applied once daily directly to the skin. As with the treatment of skin conditions, it is essential to use the cream as directed by your healthcare professional to avoid skin irritation or other side effects. Avoiding contact with the eyes, mouth, and other mucous membranes is also important.
If you have any questions about how to use this medication, please consult with your healthcare professional. They can provide you with the most accurate and personalized advice based on your specific condition and needs.
Naltrexone HCl 0.1% Topical Cream is a semisolid preparation of the medication Naltrexone, designed to be applied on the skin. It is dispensed in a pump mechanism for convenient and controlled application.
The pump mechanism is designed to provide a convenient and controlled way to apply the cream. It ensures that the right amount of cream is dispensed each time, reducing the risk of over or under-dosing.
When applied to the skin, the active ingredient Naltrexone is absorbed into the body where it works to block the effects of opioids. This can help to reduce cravings and withdrawal symptoms in individuals with opioid dependence.
The cream should be applied to clean, dry skin. Use the pump to dispense the cream and then gently rub it into the skin until it is fully absorbed. Do not apply to broken or irritated skin.
It is generally safe to apply the cream to most parts of the body. However, avoid applying it to the face, eyes, or mucous membranes. If you have any specific concerns, consult your healthcare provider.
Side effects can include skin irritation, redness, or rash at the application site. If you experience any severe or persistent side effects, contact your healthcare provider immediately.
Yes, you can use other skincare products while using this cream. However, it is recommended to apply the Naltrexone cream first and let it fully absorb before applying other products.
If you are pregnant or breastfeeding, you should consult your healthcare provider before using this cream. The effects of Naltrexone on a developing baby or nursing infant are not fully known.
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 cream to make up for a missed dose.
Store the cream at room temperature, away from heat and direct light. Do not freeze. Keep out of the reach of children and pets.
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.
Search by NCPDP 4106882, or by name and ZIP: Bayview Pharmacy, Warwick, RI 02886. Select it as the destination pharmacy and save it as a favorite. Click any value to copy it.
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)
