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Diphenhydramine HCl 2%/Naltrexone HCl 0.2% Topical Gel (Vet) is a semisolid formulation dispensed through a pump mechanism. This allows for easy and precise application on the skin, providing targeted treatment for conditions such as Atopic Dermatitis, Pruritus, Allergic Skin Reactions, Insect Bites, and Acral Lick Granuloma in veterinary patients. The gel-like consistency ensures optimal absorption of the active ingredients.
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 gel formulation of Diphenhydramine HCl 2%/Naltrexone HCl 0.2% (Vet) for the management of a variety of skin conditions in animals.
The Diphenhydramine HCl component of this formulation is an antihistamine that works to alleviate itching and inflammation associated with these conditions. On the other hand, Naltrexone HCl is an opioid antagonist that aids in reducing the compulsion to lick or scratch the affected area. The combination of these two active ingredients creates a potent solution for addressing skin conditions in animals.
This topical gel formulation is a semisolid preparation dispensed through a pump mechanism, facilitating easy and precise application on the skin for targeted treatment or absorption of active ingredients. Its gel-like consistency ensures that the medication stays where it's applied, providing maximum benefit while minimizing potential side effects.
It is crucial to adhere to the instructions provided by your veterinarian when using this product to ensure its effectiveness and the safety of your pet. If you have any queries or concerns about using this formulation, we at Bayview Pharmacy are here to assist you. We are committed to providing quality compounded medications to meet the unique needs of each animal patient.
This compounded formulation of Diphenhydramine HCl 2%/Naltrexone HCl 0.2% Topical Gel (Vet) is a semisolid preparation designed for easy and precise application on the skin. It is primarily used in the veterinary field for the treatment of various skin conditions such as Atopic Dermatitis, Pruritus, Allergic Skin Reactions, Insect Bites, and Acral Lick Granuloma.
Diphenhydramine HCl, one of the active ingredients in this formulation, is an antihistamine that functions by inhibiting the action of histamine, a substance in the body that triggers allergic symptoms. On the other hand, Naltrexone HCl is an opioid antagonist that works by blocking the effects of opioids, including endorphins. This can help reduce itching and inflammation associated with the aforementioned skin conditions.
When used in combination, these two medications can provide significant relief from the symptoms associated with these conditions. However, it is crucial to note that this formulation should not be used in patients with a known hypersensitivity to either of the active ingredients. Patients should also be closely monitored for signs of an allergic reaction, such as hives, swelling, or difficulty breathing. If any of these symptoms occur, the patient should immediately discontinue use and seek medical attention.
It is always recommended to consult with a healthcare professional or a veterinarian before starting any new medication regimen. They can provide guidance based on the patient's specific condition and medical history. If you have any questions or concerns about this formulation or its use, please consult with a healthcare professional.
This compounded formulation of Diphenhydramine HCl 2% and Naltrexone HCl 0.2% Topical Gel is specifically designed for veterinary use. The Diphenhydramine HCl component serves as an antihistamine, effectively reducing the body's allergic response. On the other hand, Naltrexone HCl is an opioid antagonist that aids in reducing inflammation. The combination of these two active ingredients works synergistically to alleviate itching, inflammation, and other symptoms associated with conditions such as atopic dermatitis, pruritus, allergic skin reactions, insect bites, and acral lick granuloma.
The gel is dispensed through a pump mechanism, which allows for easy and precise application on the skin. Once applied, the gel is rapidly absorbed into the skin, providing quick relief from discomfort. It is crucial to remember that this formulation is intended for topical use only and should not be ingested. Always follow the instructions provided by your veterinarian when using this product to ensure the safety and effectiveness of the treatment.
If you have any queries about this formulation or its potential benefits in treating atopic dermatitis, pruritus, allergic skin reactions, insect bites, or acral lick granuloma, please do not hesitate to contact us. We are committed to helping you find the most suitable treatment option for your pet's specific needs.
This Diphenhydramine HCl 2%/Naltrexone HCl 0.2% topical gel is a compounded formulation designed for veterinary use. It is a semi-solid preparation that is dispensed through a pump mechanism, allowing for easy and precise application on the skin. The gel-like consistency ensures targeted treatment or absorption of the active ingredients.
The formulation has been effectively used in the treatment of various skin conditions in animals, including Atopic Dermatitis, Pruritus, Allergic Skin Reactions, Insect Bites, and Acral Lick Granuloma. It has also shown efficacy in treating other skin conditions such as contact dermatitis, hives, and eczema. The active ingredients in the formulation work to reduce inflammation and itching associated with these conditions.
It is crucial to note that this formulation should not be applied to open wounds or areas of the skin that are broken or irritated. Potential side effects may include skin irritation or a burning sensation upon application. If any of these side effects occur, it is recommended to discontinue use and contact a healthcare provider. Furthermore, this formulation should not be used in conjunction with other topical medications.
As with any medication, it is important to use this formulation responsibly and under the guidance of a healthcare provider. If you have any questions or concerns about the use of this formulation, it is advised to consult with a healthcare professional.
This is a compounded formulation of two active ingredients, Diphenhydramine HCl and Naltrexone HCl, in a gel form. It is designed for topical application on animals and is dispensed through a pump mechanism.
The pump mechanism facilitates easy and precise application of the gel on the skin. This ensures that the correct amount of medication is applied each time.
The gel has a semisolid consistency, which allows it to stay on the skin for targeted treatment or absorption of the active ingredients.
The gel works by delivering the active ingredients directly to the area of the skin where it is applied. This allows for targeted treatment and absorption of the medication.
The active ingredients in this gel are Diphenhydramine HCl and Naltrexone HCl. Diphenhydramine HCl is an antihistamine that can help reduce itching and inflammation, while Naltrexone HCl is an opioid antagonist that can help manage pain and addiction.
This gel should be stored at room temperature, away from heat and direct sunlight. It should also be kept out of reach of children and pets.
If your pet has a reaction to this gel, such as redness, swelling, or difficulty breathing, you should stop using the gel and contact your vet immediately.
This gel is designed for use on a variety of animals, but it is always best to consult with your vet before starting any new medication regimen.
The frequency of application will depend on the specific needs of your pet and the instructions provided by your vet. Always follow the vet's instructions for use.
If you miss a dose, apply the missed dose as soon as you remember. However, if it is almost time for the next dose, skip the missed dose and continue with your regular dosing schedule. Do not apply a double dose to make up for a missed one.
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)
