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Naltrexone HCl 0.5% Topical Gel is a semisolid formulation, dispensed through a pump mechanism for easy and precise application. This medication is used for targeted treatment of alcoholism, opioid addiction, substance abuse, smoking cessation, and gambling addiction, delivering active ingredients directly through the skin in a gel-like consistency.
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% Topical Gel is a specially compounded medication that has been effectively used in the treatment of various dermatological conditions such as Vulvodynia, Lichen Sclerosus, Lichen Planus, Genital Herpes, and Pruritus Vulvae. This unique formulation is a semisolid gel that is dispensed through a pump mechanism, allowing for easy and precise application directly onto the skin of the affected area.
The active ingredient, Naltrexone HCl, works by blocking the opioid receptors in the skin, thereby reducing inflammation and pain. It also inhibits the production of inflammatory cytokines, which are proteins that can exacerbate the symptoms associated with these conditions. This dual-action mechanism has been found to not only alleviate symptoms such as itching, burning, and pain, but also to reduce the recurrence of these symptoms, providing patients with long-term relief.
For patients prescribed with Naltrexone HCl 0.5% Topical Gel, it is crucial to adhere to the instructions provided by their healthcare provider. The medication should be used as directed, avoiding contact with the eyes, mouth, and other mucous membranes. It is also advised not to apply this medication on broken or irritated skin to prevent any potential adverse reactions.
Regular monitoring of patients for any adverse reactions or changes in symptoms is recommended to ensure the medication's efficacy and the patient's safety.
If you have any questions or require further information about Naltrexone HCl 0.5% Topical Gel or its use in treating these conditions, please do not hesitate to contact us at Bayview Pharmacy. Our team of compounding pharmacists is equipped with the knowledge and expertise to assist you.
This compounded formulation of Naltrexone HCl 0.5% Topical Gel is a semisolid preparation that is dispensed through a pump mechanism. This design allows for easy and precise application on the skin, targeting the treatment area or facilitating absorption of the active ingredients in a gel-like consistency. It has been utilized in the management of conditions such as Vulvodynia, Lichen Sclerosus, Lichen Planus, Genital Herpes, and Pruritus Vulvae.
It is crucial to understand that this formulation is not specifically indicated for the treatment of these conditions. Its use should be under the guidance and direction of a healthcare provider. Naltrexone HCl 0.5% Topical Gel may help alleviate symptoms associated with these conditions, such as itching, burning, and pain. However, it should not be used as a substitute for other treatments prescribed by a healthcare provider.
When using Naltrexone HCl 0.5% Topical Gel, it is essential to adhere to the directions provided by your healthcare provider. Typically, a thin layer of the gel is applied to the affected area twice daily, or as directed by your healthcare provider. Avoid contact with the eyes, mouth, and other mucous membranes. In case of accidental contact, rinse the area thoroughly with water.
Be aware that Naltrexone HCl 0.5% Topical Gel may cause skin irritation, redness, or burning. If these side effects occur, discontinue use and contact your healthcare provider immediately. Furthermore, this formulation may interact with other medications. Therefore, it is crucial to discuss all medications and supplements you are currently taking with your healthcare provider before starting this treatment.
If you have any questions or concerns about using Naltrexone HCl 0.5% Topical Gel to manage Vulvodynia, Lichen Sclerosus, Lichen Planus, Genital Herpes, or Pruritus Vulvae, please do not hesitate to reach out to your healthcare provider for further information and guidance.
Naltrexone HCl 0.5% Topical Gel is a specially compounded medication designed to address a range of skin conditions. This includes Vulvodynia, Lichen Sclerosus, Lichen Planus, Genital Herpes, and Pruritus Vulvae. The active ingredient, Naltrexone HCl, is an opioid antagonist that functions by blocking the opioid receptors in the skin. This action helps to alleviate inflammation and pain.
The gel is applied directly to the affected area, where it is absorbed through the skin. It is typically recommended for application twice daily, with noticeable effects often appearing within a few days. The gel's semisolid formulation is dispensed through a pump mechanism, which allows for easy and precise application, ensuring targeted treatment.
For those suffering from Vulvodynia, Naltrexone HCl 0.5% Topical Gel can help to mitigate the burning and stinging sensations that are characteristic of the condition. In the case of Lichen Sclerosus and Lichen Planus, the gel can help to alleviate the itching and discomfort associated with these conditions. For individuals with Genital Herpes, the gel can help to reduce the pain and itching that accompany the condition. For Pruritus Vulvae, the gel can help to alleviate the itching and discomfort associated with this condition.
Generally, Naltrexone HCl 0.5% Topical Gel is well tolerated, with minimal side effects. However, it is crucial to adhere to the instructions provided by your healthcare provider when using this medication. If you have any questions or concerns about using this medication, it is recommended that you consult with your healthcare provider or pharmacist.
Naltrexone HCl 0.5% Topical Gel is a compounded formulation that has been extensively researched for its potential applications in a wide range of conditions. Its primary uses include the treatment of alcoholism, opioid addiction, substance abuse, smoking cessation, and gambling addiction. However, its therapeutic benefits may extend beyond these areas. It has been studied for its potential use in managing chronic pain, depression, and anxiety, offering a non-invasive alternative for patients.
Furthermore, Naltrexone HCl 0.5% Topical Gel has been explored for its potential benefits in treating various skin conditions. These include psoriasis, eczema, and acne, where it may help to alleviate symptoms and improve skin health. The gel has also been researched for its potential use in treating hair loss and alopecia, providing a topical solution that can be easily applied to the affected areas.
Generally, Naltrexone HCl 0.5% Topical Gel is well-tolerated with few reported side effects. However, as with any treatment, it is crucial to discuss potential risks and benefits with your healthcare provider before starting the regimen. This ensures that the treatment is suitable for your specific needs and circumstances. If you have any questions or concerns about the use of Naltrexone HCl 0.5% Topical Gel for any condition, it is recommended to seek professional advice.
Naltrexone HCl 0.5% Topical Gel is a semisolid formulation of the medication Naltrexone. It is dispensed through a pump mechanism for easy and precise application on the skin. The active ingredients are absorbed through the skin, providing targeted treatment.
The pump mechanism allows for easy and precise application of the gel. Simply press down on the pump to dispense the desired amount of gel.
The gel has a semisolid, gel-like consistency. This allows it to be easily spread on the skin for optimal absorption of the active ingredients.
Apply the gel to the targeted area of the skin as directed by your healthcare provider. The pump mechanism allows for precise application.
It's best to use this gel on the area directed by your healthcare provider. If you're unsure, please consult with your healthcare provider before application.
Naltrexone is the active ingredient in this gel. It's a medication that's used for various treatments, including addiction. In this topical form, it's absorbed through the skin for targeted treatment.
If you miss a dose, apply it as soon as you remember. If it's close to the time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not apply two doses at the same time.
As with any medication, there can be side effects. Common side effects may include skin irritation at the application site. If you experience any severe or persistent side effects, contact your healthcare provider immediately.
Before using other skincare products, consult with your healthcare provider. Some products may interfere with the absorption of the active ingredients in the gel.
Store the gel at room temperature, away from heat and direct light. Do not freeze. Keep out of the reach of children.
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.
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)
