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Naltrexone HCl 1% Topical Cream is a semisolid preparation, dispensed via a pump mechanism for easy and controlled application. It is designed for localized treatment of various skin conditions such as Alopecia Areata, Psoriasis, Lichen Planus, Atopic Dermatitis, and Acne Vulgaris, facilitating the absorption of active ingredients directly through the skin.
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 1% Topical Cream is a specially compounded medication designed to address a range of disease states. This unique formulation combines naltrexone hydrochloride, a synthetic opioid antagonist, with a topical cream base, creating a potent solution for treating conditions such as psoriasis, eczema, and other skin-related ailments.
The cream works by blocking the opioid receptors in the skin, which in turn helps to reduce inflammation and pain. It also aids in alleviating itching and redness associated with these conditions. The cream is dispensed in a pump mechanism, designed for convenient and controlled application on the skin for localized treatment or absorption of active ingredients. This ensures that the medication is applied directly to the affected area, providing targeted relief.
As a appropriate treatment option, Naltrexone HCl 1% Topical Cream offers significant benefits to patients suffering from psoriasis, eczema, and other skin conditions. However, it is crucial to use this medication as directed by a healthcare provider. Misuse or overuse can lead to unwanted side effects or reduced effectiveness of the treatment.
If you have any questions or concerns about this formulation or its application, we encourage you to reach out to your healthcare provider or pharmacist. They can provide you with the necessary guidance and instructions to ensure you get the most benefit from this treatment. Remember, your health and well-being are our top priority.
Naltrexone HCl 1% Topical Cream is a compounded formulation designed for localized treatment of various disease states. This semisolid preparation is dispensed through a pump mechanism, ensuring a convenient and controlled application on the skin. It is crucial to understand that this formulation is not suitable for individuals with a known hypersensitivity to naltrexone or any other ingredients present in the cream.
Furthermore, this formulation should not be used in conjunction with other topical medications. Doing so may heighten the risk of adverse effects. It is also noteworthy that this formulation may interact with certain medications, including but not limited to opioids, benzodiazepines, and alcohol. Therefore, it is strongly advised to discuss any current medications with a healthcare provider before initiating the use of this formulation.
Patients should also be cognizant of the fact that this formulation may cause skin irritation, redness, or itching. In the event of any of these symptoms, it is recommended to discontinue use immediately and consult with a healthcare provider. It is always important to stay informed and communicate openly with your healthcare provider to ensure the safe and appropriate use of this medication.
Naltrexone HCl 1% Topical Cream is a specially compounded prescription medication designed to treat a range of skin conditions, including psoriasis, eczema, and atopic dermatitis. The cream's active ingredient, naltrexone hydrochloride, is a synthetic opioid antagonist. It functions by blocking the effects of opioid receptors in the skin, thereby reducing inflammation and itching associated with various skin conditions.
When applied topically, Naltrexone HCl 1% Topical Cream is absorbed through the skin and enters the bloodstream. Here, it binds to opioid receptors and inhibits their effects, further helping to alleviate inflammation and itching. The cream is typically applied to the affected area twice daily, or as directed by a healthcare provider. It is crucial to adhere to the instructions on the product label and use the medication as directed.
While applying the cream, it is important to avoid contact with the eyes, mouth, and other mucous membranes. Naltrexone HCl 1% Topical Cream is generally well tolerated, but some individuals may experience side effects such as burning, stinging, or redness at the application site. If these or any other side effects occur, it is recommended to contact a healthcare provider immediately.
If you have any questions or concerns about using Naltrexone HCl 1% Topical Cream, don't hesitate to reach out to your healthcare provider or pharmacist.
Naltrexone HCl 1% Topical Cream is a semisolid preparation of the medication Naltrexone, designed for application on the skin. It is dispensed in a pump mechanism for convenient and controlled application.
Naltrexone HCl 1% Topical Cream works by delivering the active ingredient, Naltrexone, directly to the area of the skin where it is applied. This allows for localized treatment or absorption of the medication.
You should apply Naltrexone HCl 1% Topical Cream as directed by your healthcare provider. The pump mechanism allows for controlled application, so you can easily apply the correct amount of cream to the affected area.
It's important to use Naltrexone HCl 1% Topical Cream only as directed by your healthcare provider. While it is designed for skin application, some areas of the body may be more sensitive than others. Always follow your healthcare provider's instructions.
As with any medication, Naltrexone HCl 1% Topical Cream can have side effects. These can include skin irritation at the application site. If you experience any unusual or severe side effects, contact your healthcare provider immediately.
If you are pregnant or breastfeeding, you should discuss the use of Naltrexone HCl 1% Topical Cream with your healthcare provider. They can provide guidance based on your specific situation and the potential risks and benefits of the medication.
Before using other skin products in combination with Naltrexone HCl 1% Topical Cream, it's important to discuss this with your healthcare provider. Some products may interfere with the absorption or effectiveness of the medication.
Naltrexone HCl 1% Topical Cream should be stored at room temperature, away from heat and direct light. Keep the container tightly closed when not in use.
If you miss a dose of Naltrexone HCl 1% Topical Cream, apply it as soon as you remember. However, if it's close to the time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not apply extra cream to make up for a missed dose.
If you believe you have applied too much Naltrexone HCl 1% Topical Cream, contact your healthcare provider or local poison control center immediately. Symptoms of an overdose may include severe skin irritation or other unusual symptoms.
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)
