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Bayview Pharmacy's Phenytoin 2%/Arginine HCl 1%/Naltrexone HCl 0.5%/Timolol 0.5% Topical Gel is a unique compounded formulation. This semisolid medication is dispensed through a pump mechanism, ensuring easy and accurate application on the skin. It is designed for targeted treatment or absorption of active ingredients, offering potential relief for conditions such as epilepsy, glaucoma, multiple sclerosis, Parkinson's disease, and neuropathic pain.
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 Phenytoin 2%/Arginine HCl 1%/Naltrexone HCl 0.5%/Timolol 0.5%. This unique blend is specifically designed to address a range of skin conditions such as psoriasis, eczema, and acne. The active ingredients work synergistically to alleviate inflammation, diminish redness, and lessen the visibility of lesions.
The Phenytoin component in the formulation serves to mitigate itching and irritation, while the Arginine HCl works to alleviate inflammation and redness. The Naltrexone HCl is instrumental in reducing the visibility of lesions, and the Timolol aids in controlling the production of sebum, a common contributor to acne.
This formulation is a potent solution for various skin conditions and is designed for ease of use. It is dispensed through a pump mechanism, facilitating precise application on the skin for targeted treatment. The gel-like consistency ensures optimal absorption of the active ingredients. Patients are advised to apply the gel to the affected area twice daily, adhering to the recommended dosage to ensure safety and effectiveness.
While this formulation is generally well-tolerated, it may cause skin irritation in some individuals. Patients are advised to discontinue use and consult their healthcare provider if any irritation occurs. It is also important to note that this formulation is not recommended for use in pregnant or breastfeeding women. Additionally, caution is advised for patients with a history of skin allergies.
If you have any questions about this formulation or its application in treating skin conditions, please do not hesitate to contact us.
Phenytoin 2%/Arginine HCl 1%/Naltrexone HCl 0.5%/Timolol 0.5% Topical Gel is a compounded formulation designed for topical application. It is indicated for the treatment of various skin conditions, including psoriasis, eczema, and atopic dermatitis. The unique combination of active ingredients works synergistically to alleviate symptoms associated with these conditions. Phenytoin and Arginine HCl work together to reduce inflammation and itching, while Naltrexone HCl and Timolol 0.5% help to minimize redness and swelling. This formulation has also shown efficacy in treating acne, rosacea, and other skin conditions.
Patients should be aware that this formulation may cause skin irritation, redness, or a burning sensation. If any of these side effects occur, it is recommended to discontinue use and contact a healthcare provider. It is also important to note that this formulation may interact with other medications, including anticoagulants, anti-seizure medications, and immunosuppressants. Therefore, patients should inform their healthcare provider of any medications they are currently taking before starting this treatment.
Prescribers should be aware that this formulation should not be used in patients with a known hypersensitivity to any of the ingredients. Additionally, it is contraindicated in patients with a history of glaucoma, heart disease, or liver or kidney disease. It is crucial to conduct a thorough medical history and examination before prescribing this formulation to ensure patient safety.
If you have any questions or concerns about this formulation or its use, please do not hesitate to reach out to your healthcare provider for further information and guidance.
Phenytoin 2%/Arginine HCl 1%/Naltrexone HCl 0.5%/Timolol 0.5% Topical Gel is a compounded formulation designed to address a range of skin conditions. This unique blend of four active ingredients each plays a crucial role in managing skin health. Phenytoin, an anticonvulsant, is instrumental in reducing inflammation and itching. Arginine HCl, an amino acid, aids in minimizing redness and swelling. Naltrexone HCl, an opioid antagonist, contributes to pain and itch relief. Lastly, Timolol, a beta-blocker, assists in reducing redness and swelling.
When applied topically, this formulation penetrates the skin to deliver the active ingredients directly to the affected area. The ingredients are then absorbed into the skin, where they work synergistically to alleviate inflammation, itching, redness, and swelling. The typical application of this formulation is twice daily, or as directed by a healthcare provider.
This versatile formulation can be used to treat a variety of skin conditions, including but not limited to eczema, psoriasis, and contact dermatitis. The semisolid formulation is dispensed through a pump mechanism, which allows for easy and precise application, ensuring targeted treatment and optimal absorption of the active ingredients.
If you have any questions about this formulation or its application, please do not hesitate to reach out.
This compounded formulation is designed to deliver targeted treatment through the skin. It contains Phenytoin, Arginine HCl, Naltrexone HCl, and Timolol, which work together to treat a variety of conditions.
This gel is dispensed through a pump mechanism for easy and precise application. Simply apply it to the affected area as directed by your healthcare provider.
The gel has a semisolid formulation, which means it is not as liquid as a lotion but not as solid as a cream. This consistency allows for easy application and absorption through the skin.
The active ingredients in this formulation are Phenytoin 2%, Arginine HCl 1%, Naltrexone HCl 0.5%, and Timolol 0.5%.
Each active ingredient plays a unique role. Phenytoin is often used to control seizures, Arginine HCl is an amino acid that may promote wound healing, Naltrexone HCl is used to manage alcohol or opioid dependence, and Timolol is a beta-blocker that can reduce pressure inside the eye.
It's best to use this gel only on the area of the skin as directed by your healthcare provider. Avoid contact with eyes, mouth, and other sensitive areas.
If you experience any side effects, such as skin irritation or allergic reactions, stop using the gel and contact your healthcare provider immediately.
Store this gel at room temperature, away from heat and direct light. Do not freeze. Keep out of the reach of children and pets.
If you are pregnant or breastfeeding, consult your healthcare provider before using this gel. Some ingredients may pass into breast milk and may have undesirable effects on a nursing infant.
If you miss a dose, apply it as soon as you remember. However, if it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.
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.
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)
