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Naltrexone HCl 0.5%/Azelastine HCl 0.1% Topical Gel is a compounded, semisolid formulation dispensed through a pump mechanism. This allows for easy and precise application on the skin, targeting the treatment or absorption of active ingredients. It is used to treat conditions such as Allergic Rhinitis, Atopic Dermatitis, Pruritus, Urticaria, and Contact Dermatitis.
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 0.5%/Azelastine HCl 0.1% Topical Gel is a specially compounded medication designed to address a range of skin conditions. This unique formulation combines the potent effects of naltrexone hydrochloride, an opioid antagonist known for its ability to alleviate inflammation and itching, and azelastine hydrochloride, an antihistamine that effectively reduces redness and swelling. The combined action of these two active ingredients makes this topical gel a powerful treatment option for various skin conditions, including but not limited to eczema, psoriasis, and contact dermatitis.
This semisolid formulation 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, providing relief exactly where it's needed.
At Bayview Pharmacy, we take pride in offering this compounded formulation to our patients. Our team of compounding pharmacists brings a wealth of experience in creating customized medications to cater to the unique needs of each patient.
If you have any questions about Naltrexone HCl 0.5%/Azelastine HCl 0.1% Topical Gel or any of our other compounded medications, we encourage you to reach out to us. Our team of compounding pharmacists is always ready to assist you in finding the best treatment for your condition.
Naltrexone HCl 0.5%/Azelastine HCl 0.1% Topical Gel is a compounded formulation designed for the treatment of mild to moderate atopic dermatitis, psoriasis, and seborrheic dermatitis. This semisolid formulation is dispensed through a pump mechanism, allowing for easy and precise application on the skin. The active ingredients in the gel work to target and alleviate symptoms such as itching, redness, and inflammation associated with these skin conditions.
It is recommended that patients apply the gel twice daily, or as directed by their healthcare provider.
Patients should be aware that this medication may cause local skin reactions such as burning, stinging, itching, or redness. If these reactions occur, patients should contact their healthcare provider immediately. Additionally, this medication may cause drowsiness or blurred vision. As such, patients should refrain from driving or operating machinery until they understand how this medication affects them.
It is important to avoid contact with the eyes, nose, and mouth when applying this medication. If contact occurs, the area should be rinsed with water immediately. Patients should also avoid exposure to sunlight or artificial UV light while using this medication due to potential photosensitivity reactions.
Patients should also be aware that this medication may interact with other medications they are taking. It is crucial that patients inform their healthcare provider of all medications they are currently taking, including over-the-counter medications, vitamins, and herbal supplements, to avoid potential drug interactions.
If you have any questions about using Naltrexone HCl 0.5%/Azelastine HCl 0.1% Topical Gel, please do not hesitate to reach out to your healthcare provider for further information and guidance.
Naltrexone HCl 0.5%/Azelastine HCl 0.1% Topical Gel is a compounded formulation designed to address a range of skin conditions such as eczema, psoriasis, and atopic dermatitis. This unique combination of active ingredients, naltrexone hydrochloride and azelastine hydrochloride, synergistically work to alleviate inflammation and itching associated with these skin conditions.
Naltrexone hydrochloride is an opioid antagonist that functions by blocking the action of specific opioid receptors in the body. This action helps to reduce the sensation of itching often experienced with skin conditions. On the other hand, azelastine hydrochloride is an antihistamine that inhibits the action of histamine, a substance released by the body during an allergic reaction, thereby reducing inflammation.
The gel is dispensed through a pump mechanism, which allows for easy and precise application on the skin. This targeted treatment ensures that the active ingredients are delivered directly to the affected area, enhancing their effectiveness. It is crucial to follow the instructions provided by your healthcare provider when using this medication. Typically, the gel should be applied to the affected area twice daily, or as directed by your healthcare provider. Always remember to wash your hands before and after applying the gel, and avoid applying it to broken or irritated skin.
If you have any questions or concerns about using Naltrexone HCl 0.5%/Azelastine HCl 0.1% Topical Gel, please do not hesitate to contact us at Bayview Pharmacy. We are committed to helping you understand your medication and achieve the best possible outcomes from your treatment.
This is a compounded formulation of two active ingredients, Naltrexone HCl and Azelastine HCl, in a semisolid gel form. It is designed for easy and precise application on the skin for targeted treatment.
The pump mechanism allows for easy dispensing of the gel. It ensures that the right amount of the formulation is dispensed each time, ensuring accurate dosing and application.
You should apply the gel directly to the affected area of the skin as directed by your healthcare provider. The pump mechanism will dispense the correct amount of gel for application.
The gel-like consistency allows for easy application and absorption of the active ingredients into the skin. It also helps to keep the medication in place, providing targeted treatment to the specific area where it is applied.
The active ingredients in this formulation are Naltrexone HCl at a concentration of 0.5% and Azelastine HCl at a concentration of 0.1%.
Naltrexone HCl is an opioid antagonist. It is used in this formulation for its potential benefits in reducing inflammation and pain.
Azelastine HCl is an antihistamine. It is used in this formulation for its potential benefits in reducing allergic reactions and inflammation.
This gel is designed for topical use and can be applied to most areas of the body. However, it should not be used on broken or irritated skin, or near the eyes or mouth. Always follow your healthcare provider's instructions.
If you experience any side effects, such as skin irritation or allergic reactions, stop using the gel and contact your healthcare provider immediately.
Store the gel 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.
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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)
