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Bayview Pharmacy's Ketamine HCl 1%/Naltrexone HCl 0.1% 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, Pyoderma, Acral Lick Granuloma, and Interdigital Cysts in animals. 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 Ketamine HCl 1%/Naltrexone HCl 0.1% designed for the treatment of various dermatological conditions in veterinary patients. This unique formulation has demonstrated efficacy in treating conditions such as Atopic Dermatitis, Pruritus, Allergic Skin Disease, Acral Lick Granuloma, and Interdigital Cysts.
Ketamine HCl, an NMDA receptor antagonist, has been a staple in veterinary medicine for many years due to its analgesic and sedative properties. Naltrexone HCl, an opioid receptor antagonist, has been utilized in human medicine to treat opioid addiction. The combination of these two drugs in a topical gel formulation has shown promising results in treating a range of dermatological conditions in veterinary patients.
This semisolid formulation is dispensed through a pump mechanism, facilitating easy and precise application on the skin for targeted treatment or absorption of active ingredients in a gel-like consistency. The topical gel formulation of Ketamine HCl 1%/Naltrexone HCl 0.1% is designed for direct application to the affected area as directed by a veterinarian. It is important to note that this gel should not be used on open wounds or on areas of the skin that are broken or irritated.
If you have any queries about this formulation or its application in treating Atopic Dermatitis, Pruritus, Allergic Skin Disease, Acral Lick Granuloma, or Interdigital Cysts, please do not hesitate to contact us at Bayview Pharmacy. Our team is committed to providing the best treatment options for your veterinary patients and is ready to assist with any questions you may have.
This compounded formulation of Ketamine HCl 1%/Naltrexone HCl 0.1% Topical Gel is a semisolid preparation designed for veterinary use. It 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.
The topical gel is indicated for the treatment of Atopic Dermatitis, Pruritus, Allergic Skin Disease, Acral Lick Granuloma, and Interdigital Cysts in veterinary patients. Ketamine HCl, an NMDA receptor antagonist, and Naltrexone HCl, an opioid receptor antagonist, work in synergy to reduce inflammation and pruritus associated with these conditions.
It is crucial to monitor patients for signs of adverse reactions, such as skin irritation, redness, or swelling. If any of these signs are observed, the medication should be discontinued and the prescriber notified. Similarly, signs of infection, such as fever, chills, or pus, should be closely monitored. If any of these signs are observed, the medication should be discontinued and the prescriber notified.
This medication should not be used in patients who are pregnant or nursing. Additionally, it should not be used in patients who are allergic to any of the ingredients in the formulation. If you have any questions about this formulation or its use in treating Atopic Dermatitis, Pruritus, Allergic Skin Disease, Acral Lick Granuloma, or Interdigital Cysts, please reach out for further information.
Ketamine HCl 1%/Naltrexone HCl 0.1% Topical Gel (Vet) is a specially compounded formulation designed to address a range of skin conditions in animals. This unique combination of ketamine, an anesthetic that blocks nerve signals in the brain, and naltrexone, an opioid antagonist that mitigates the effects of opioids on the body, works synergistically to alleviate inflammation, itching, and pain associated with various skin conditions.
This topical gel is indicated for a variety of skin conditions in animals, including but not limited to atopic dermatitis, pruritus, allergic skin disease, acral lick granuloma, and interdigital cysts. The gel is applied directly to the affected skin area as per the veterinarian's instructions. It is crucial to note that this gel should not be applied to open wounds or areas of the skin that are broken or irritated.
When administering Ketamine HCl 1%/Naltrexone HCl 0.1% Topical Gel (Vet), it is essential to adhere to the directions provided by your veterinarian. The gel should be applied directly to the affected skin area as instructed. Care should be taken to avoid contact with the eyes, nose, and mouth of the animal. In case of accidental contact with the eyes, rinse thoroughly with water and seek immediate veterinary attention if irritation persists.
If you have any queries or concerns about using Ketamine HCl 1%/Naltrexone HCl 0.1% Topical Gel (Vet) to treat atopic dermatitis, pruritus, allergic skin disease, acral lick granuloma, or interdigital cysts, please do not hesitate to reach out. We are committed to providing the best possible treatment options for your pet's health and well-being.
This compounded formulation of Ketamine HCl 1%/Naltrexone HCl 0.1% Topical Gel (Vet) is a semisolid formulation designed for easy and precise application on the skin of animals. It is dispensed through a pump mechanism, ensuring targeted treatment or absorption of active ingredients in a gel-like consistency. This formulation is specifically indicated for the treatment of Atopic Dermatitis, Pruritus, Pyoderma, Acral Lick Granuloma, and Interdigital Cysts in animals.
While it is primarily used for these conditions, it may also be beneficial in treating other skin conditions in animals, such as bacterial and fungal infections, as well as other inflammatory skin conditions. Additionally, it may be used to alleviate pain associated with these conditions. However, it is crucial to note that this formulation should not be used in animals with known hypersensitivity to either of the active ingredients, Ketamine HCl or Naltrexone HCl.
This formulation is strictly for veterinary use and should not be used in humans. It is essential to follow the instructions of the veterinarian when using this product to ensure the safety and well-being of the animal. If you have any questions or concerns about the use of this formulation, please do not hesitate to reach out. Our team of compounding pharmacists is here to assist you.
This is a compounded formulation of Ketamine HCl and Naltrexone HCl in a gel form. It is a semisolid formulation that is dispensed through a pump mechanism for easy and precise application on the skin.
The pump mechanism facilitates easy and precise application of the gel on the skin. It ensures that the right amount of gel is dispensed each time, reducing the risk of over or under-dosing.
The gel has a semisolid, gel-like consistency. This makes it easy to apply and allows for targeted treatment or absorption of the active ingredients.
This gel is applied topically on the skin. The pump mechanism allows for easy and precise application, ensuring that the active ingredients are delivered to the targeted area.
The active ingredients in this gel are Ketamine HCl and Naltrexone HCl. These are compounded together in a semisolid formulation for topical application.
Ketamine HCl is a powerful anesthetic that can provide pain relief. When applied topically, it can help to numb the targeted area and reduce discomfort.
Naltrexone HCl is an opioid antagonist. It can help to block the effects of opioids and can be used to treat opioid dependence or addiction.
This gel is intended for veterinary use. However, it should only be used under the supervision of a veterinarian and is not suitable for all animals. Always consult with a veterinarian before using this gel on your pet.
It is not recommended to use this gel on broken or irritated skin. If your pet has any skin conditions or injuries, please consult with a veterinarian before using this gel.
If your pet has a reaction to this gel, stop using it immediately and consult with a veterinarian. Reactions can include redness, irritation, or other signs of discomfort.
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.
This preparation is a controlled substance. Additional prescribing, refill, and shipping restrictions apply, and the states Bayview can dispense it to are narrower than for non-controlled preparations.
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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)
