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Ketamine HCl 1%/Naltrexone HCl 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 aids in the 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 1% for the management of a range of dermatological conditions in veterinary patients. This unique formulation has demonstrated efficacy in the treatment of Atopic Dermatitis, Pruritus, Allergic Skin Disease, Pyoderma, and Acral Lick Granuloma.
Ketamine HCl, an NMDA receptor antagonist, has a long-standing history of use in veterinary medicine as an anesthetic and analgesic. Its anti-inflammatory and immunomodulatory properties have been recognized, making it a potent treatment for Atopic Dermatitis, Pruritus, and Allergic Skin Disease. Naltrexone HCl, an opioid antagonist, has been employed in the treatment of opioid addiction in humans. It too has anti-inflammatory and immunomodulatory properties.
The combination of Ketamine HCl 1%/Naltrexone HCl 1% in a semisolid formulation dispensed through a pump mechanism allows for easy and precise application on the skin for targeted treatment or absorption of active ingredients in a gel-like consistency. This provides a appropriate treatment for a variety of dermatological conditions in veterinary patients.
If you have any queries about this formulation or its application in treating your patient, we encourage you to contact us. Our team is committed to providing comprehensive information and support to ensure the best possible outcomes for your patients.
This compounded formulation of Ketamine HCl 1%/Naltrexone HCl 1% Topical Gel (Vet) is a specialized treatment designed for veterinary use, specifically for conditions such as Atopic Dermatitis, Pruritus, Allergic Skin Disease, Pyoderma, and Acral Lick Granuloma. The gel is a semisolid formulation that is dispensed through a pump mechanism, allowing for easy and precise application directly onto the skin of the affected area. This targeted treatment facilitates the absorption of the active ingredients in a gel-like consistency, providing relief and treatment where it's needed most.
The combination of Ketamine HCl and Naltrexone HCl in this formulation works synergistically to reduce inflammation and itching, providing both analgesic and anti-pruritic effects. This dual-action approach helps to alleviate discomfort and promote healing in the affected areas. However, it is crucial to note that this formulation should not be used in cats or dogs with a known hypersensitivity to either of the active ingredients. It is also contraindicated in animals with a history of seizures or other neurological disorders due to the potential for adverse reactions.
As with any medication, it is essential to use this formulation under the guidance of a veterinary professional. If you have any questions or concerns about the use of this compounded formulation of Ketamine HCl 1%/Naltrexone HCl 1% Topical Gel (Vet), it is recommended to consult with a veterinary healthcare provider to ensure the safety and efficacy of the treatment for your pet's specific needs.
Ketamine HCl 1%/Naltrexone HCl 1% Topical Gel (Vet) is a compounded formulation designed for veterinary use. This semisolid formulation is dispensed through a pump mechanism, ensuring easy and precise application on the skin. It is specifically designed for targeted treatment or absorption of active ingredients in a gel-like consistency.
The formulation combines two active ingredients, ketamine hydrochloride and naltrexone hydrochloride. Ketamine hydrochloride works to alleviate inflammation and itching, while naltrexone hydrochloride aids in reducing the urge to lick or scratch the affected area.
When using this topical gel, it is crucial to adhere to the instructions provided by your veterinarian. The gel should be applied directly to the affected area twice daily, or as directed by your veterinarian. It is important to avoid contact with the eyes, nose, and mouth of the animal, and to wash your hands thoroughly after applying the gel. This careful application helps to maximize the effectiveness of the treatment while minimizing potential side effects.
As with any medication, it is important to monitor your pet's response to the treatment and report any unusual reactions or lack of improvement to your veterinarian.
This compounded formulation of Ketamine HCl 1%/Naltrexone HCl 1% Topical Gel (Vet) is a semisolid preparation designed for easy and precise application on the skin of animals. It is dispensed through a pump mechanism, which allows for targeted treatment or absorption of the active ingredients. The gel-like consistency ensures that the medication is absorbed effectively through the skin.
It has been utilized in the veterinary field to manage a range of skin conditions such as Atopic Dermatitis, Pruritus, Pyoderma, Acral Lick Granuloma, and Interdigital Cysts. The topical application allows for direct treatment of the affected area, providing relief and promoting healing.
It is crucial to understand that this formulation is specifically designed for veterinary use and should not be applied to humans. It has not undergone testing for safety and efficacy in human subjects. For any queries or concerns regarding the use of this formulation, it is recommended to consult with a veterinary professional.
This is a compounded formulation of Ketamine HCl and Naltrexone HCl in a gel form. It is designed for easy and precise application on the skin for targeted treatment or absorption of the active ingredients.
The gel is dispensed through a pump mechanism, which allows for easy and precise application on the skin.
The gel has a semisolid formulation, which means it has a gel-like consistency.
The pump mechanism facilitates easy and precise application of the gel on the skin, ensuring that the correct amount of medication is applied each time.
The active ingredients in this topical gel are Ketamine HCl and Naltrexone HCl.
The gel is applied to the skin where it is absorbed and the active ingredients, Ketamine HCl and Naltrexone HCl, provide targeted treatment.
As with any medication, it's important to consult with a veterinarian before using this product on your pet. The vet will be able to determine if this medication is safe and appropriate for your pet's specific needs.
The frequency of application will depend on the specific needs of your pet and the instructions provided by your veterinarian. Always follow the vet's instructions for use.
If your pet has a reaction to the medication, stop using it immediately and contact your veterinarian for advice.
Before using this medication in conjunction with other medications, it's important to consult with your veterinarian. They will be able to provide guidance based on your pet's specific needs and medical history.
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.
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)
