Bayview Pharmacy's Naltrexone HCl 1%/Doxepin HCl 0.5% Topical Cream is a compounded, semisolid preparation dispensed in a pump mechanism. This formulation is designed for convenient and controlled application on the skin, providing localized treatment for conditions such as Atopic Dermatitis, Psoriasis, Pruritus, Lichen Simplex Chronicus, 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 cream formulation of Naltrexone HCl 1%/Doxepin HCl 0.5%. This unique combination of medications is specifically designed to address a range of skin conditions, including psoriasis, eczema, and atopic dermatitis. The active ingredients in this formulation, Naltrexone HCl and Doxepin HCl, work synergistically to alleviate the symptoms associated with these skin conditions.
Naltrexone HCl, an opioid antagonist, plays a crucial role in reducing inflammation and itching, which are common symptoms of these skin conditions. On the other hand, Doxepin HCl, an antidepressant, aids in reducing pain and discomfort, providing relief to the affected areas. Together, these medications offer a comprehensive approach to managing and reducing the symptoms of various skin conditions.
This topical cream formulation is dispensed in a pump mechanism, ensuring a convenient and controlled application on the skin. It is designed for localized treatment, allowing for targeted absorption of the active ingredients. The cream is easy to apply and can be incorporated into your daily skincare routine. However, it is important to avoid applying this formulation on broken or irritated skin. Additionally, patients with a history of allergies or skin sensitivities should exercise caution when using this product.
If you have any queries or require further information about this formulation or its application in treating skin conditions, please do not hesitate to contact us at Bayview Pharmacy. Our team is committed to assisting you in finding the most suitable treatment option tailored to your specific needs.
Naltrexone HCl 1%/Doxepin HCl 0.5% Topical Cream is a compounded formulation designed for the treatment of skin conditions such as atopic dermatitis, psoriasis, and pruritus. This semisolid preparation is dispensed in a pump mechanism, allowing for convenient and controlled application on the skin for localized treatment or absorption of active ingredients.
The cream is a combination of two active ingredients, naltrexone and doxepin. Naltrexone is an opioid antagonist that works by blocking the action of opioid receptors, thereby reducing inflammation. On the other hand, doxepin is an antihistamine that works by blocking the action of histamine receptors, thereby reducing itching. Together, these medications work synergistically to alleviate the symptoms associated with these skin conditions.
For optimal results, Naltrexone HCl 1%/Doxepin HCl 0.5% Topical Cream should be applied to the affected area twice daily, or as directed by your healthcare provider. It is crucial to avoid contact with the eyes, mouth, and other mucous membranes. In case of accidental contact, the area should be rinsed thoroughly with water.
Patients should be aware that this medication may cause side effects such as skin irritation, redness, burning, or drowsiness. If these side effects occur, it is recommended to contact your healthcare provider immediately. Caution should also be exercised when driving or operating machinery as this medication may cause drowsiness.
It is important to note that this medication may interact with other medications, including other topical medications, anticoagulants, and certain antibiotics. Therefore, patients should inform their healthcare provider of all medications they are currently taking before starting the use of this medication.
If you have any questions or concerns about Naltrexone HCl 1%/Doxepin HCl 0.5% Topical Cream, please do not hesitate to reach out to your healthcare provider for further information and guidance.
This unique blend is designed to target and alleviate symptoms such as inflammation and itching, commonly associated with skin conditions like eczema, psoriasis, and contact dermatitis.
Naltrexone hydrochloride, an opioid antagonist, works by blocking the effects of opioids on the body. This action helps to reduce inflammation, a common symptom of many skin conditions. On the other hand, doxepin hydrochloride is an antidepressant that functions by inhibiting the reuptake of serotonin and norepinephrine in the brain. This mechanism aids in reducing itching, another prevalent symptom of skin disorders.
The Naltrexone HCl 1%/Doxepin HCl 0.5% Topical Cream is dispensed in a pump mechanism, which allows for convenient and controlled application on the skin. This ensures that the active ingredients are localized to the area of treatment, maximizing their effectiveness. The cream should be applied to the affected area twice daily, or as directed by your healthcare provider.
While Naltrexone HCl 1%/Doxepin HCl 0.5% Topical Cream is generally well tolerated, 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 your healthcare provider immediately.
If you have any questions or concerns about Naltrexone HCl 1%/Doxepin HCl 0.5% Topical Cream, or its mechanism of action, please do not hesitate to reach out.
This compounded formulation of Naltrexone HCl 1%/Doxepin HCl 0.5% is a semisolid preparation dispensed in a pump mechanism, designed for convenient and controlled application on the skin. It is primarily used for localized treatment or absorption of active ingredients. The formulation has been effectively used in the treatment of various skin conditions including atopic dermatitis, psoriasis, pruritus, lichen simplex chronicus, and acne vulgaris. It has also shown efficacy in treating contact dermatitis, seborrheic dermatitis, and neurodermatitis. This formulation is particularly beneficial for those suffering from chronic pruritus, a condition characterized by persistent itching, and prurigo nodularis, a skin condition characterized by itchy nodules. It has also been used in the management of post-herpetic neuralgia, a condition resulting from nerve damage after a shingles infection. Additionally, this formulation has been used to alleviate chronic pain conditions, such as neuropathic pain. For any queries regarding the use of this formulation for these conditions, please feel free to contact us.
This is a compounded formulation of two active ingredients, Naltrexone HCl at 1% and Doxepin HCl at 0.5%. It is a semisolid preparation designed for application on the skin for localized treatment.
The cream is dispensed in a pump mechanism, which allows for convenient and controlled application on the skin.
The pump mechanism is designed to provide a controlled amount of the cream for application, ensuring the correct dosage is used each time.
The cream should be applied topically to the skin in the area requiring treatment. The pump mechanism will dispense the correct amount of cream for each application.
The active ingredients in this cream are Naltrexone HCl at a concentration of 1% and Doxepin HCl at a concentration of 0.5%.
Naltrexone HCl is an opioid antagonist. It is used in this cream to help manage certain skin conditions by reducing inflammation and other symptoms.
Doxepin HCl is a tricyclic antidepressant with antihistamine properties. It is used in this cream to help manage itching and other symptoms associated with certain skin conditions.
Not necessarily. The cream is formulated for specific skin conditions. It is important to consult with a healthcare provider to determine if this cream is suitable for your specific condition.
As with any medication, there may be potential side effects. These can include skin irritation, redness, or itching. If you experience any severe or persistent side effects, you should contact your healthcare provider immediately.
The cream should be stored at room temperature, away from heat and direct light. Keep the container tightly closed when not in use.
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)