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Bayview Pharmacy's Zinc Oxide 12.5%/Lidocaine 5%/Pramoxine HCl 1% Topical/Rectal Gel 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 pruritus, anal fissures, hemorrhoids, anal pruritus, and anal eczema. 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's Zinc Oxide 12.5%/Lidocaine 5%/Pramoxine HCl 1% Topical/Rectal Gel is a specialized compounded formulation designed to address a range of conditions associated with the anal region.
The active ingredients in this formulation work synergistically to provide relief. Zinc Oxide, a known anti-inflammatory agent, helps to reduce inflammation and irritation. Lidocaine and Pramoxine HCl, both local anesthetics, provide a numbing effect to alleviate pain and discomfort associated with these conditions.
This semisolid formulation is dispensed through a pump mechanism, facilitating easy and precise application on the skin for targeted treatment. The gel-like consistency allows for optimal absorption of the active ingredients, enhancing the effectiveness of the treatment. This formulation can be applied both topically and rectally, providing versatile treatment options.
Bayview Pharmacy's Zinc Oxide 12.5%/Lidocaine 5%/Pramoxine HCl 1% Topical/Rectal Gel is a safe and user-friendly treatment option. Patients are advised to follow the instructions provided by their healthcare provider when using this formulation. For any queries or concerns regarding this formulation or its usage, please do not hesitate to contact us at Bayview Pharmacy.
This compounded formulation of Zinc Oxide 12.5%/Lidocaine 5%/Pramoxine HCl 1% Topical/Rectal Gel is a semisolid formulation dispensed through a pump mechanism, designed for easy and precise application on the skin. It is primarily used for the targeted treatment of pruritus, hemorrhoids, anal fissures, anal pruritus, and perianal dermatitis.
Zinc Oxide, an astringent and antiseptic, works to reduce inflammation and itching. Lidocaine, a topical anesthetic, aids in reducing pain and discomfort. Pramoxine HCl, an anti-itch medication, further helps to alleviate itching and inflammation. This combination of active ingredients works synergistically to alleviate the symptoms associated with these conditions.
Patients are advised to apply the gel to the affected area up to four times daily or as directed by their healthcare provider. It is important to avoid contact with the eyes and mucous membranes. In case of accidental contact, rinsing with water is recommended. This product should not be used for more than 7 days unless directed by a healthcare provider.
If symptoms do not improve or if any adverse reactions are experienced, patients should immediately contact their healthcare provider. Signs of infection, such as redness, swelling, or fever, should also be reported to a healthcare provider without delay.
Prescribers are advised to exercise caution when prescribing this product to patients with a known hypersensitivity to any of the ingredients. Additionally, caution should be exercised when prescribing this product to patients with a history of renal or hepatic impairment.
For any further queries or concerns, please do not hesitate to reach out to us.
This compounded formulation is a topical/rectal gel that contains 12.5% zinc oxide, 5% lidocaine, and 1% pramoxine hydrochloride. It is a semisolid formulation that 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 formulation is designed to treat a variety of conditions, including pruritus, hemorrhoids, anal fissures, anal pruritus, and perianal dermatitis. The zinc oxide present in the formulation acts as an astringent, helping to reduce inflammation and irritation. Lidocaine, a topical anesthetic, aids in reducing pain and itching. Pramoxine hydrochloride, an anti-itch medication, helps to alleviate the sensation of itching.
When using this formulation, it should be applied directly to the affected area. Care should be taken to avoid contact with the eyes, nose, and mouth. It is also recommended to wash hands thoroughly after application. The gel should be applied 2-3 times daily, or as directed by a healthcare provider.
While this formulation is generally well tolerated, some individuals may experience mild skin irritation or a burning sensation. If these symptoms occur, it is advised to discontinue use and contact a healthcare provider immediately.
If you have any questions about this formulation or its application, please do not hesitate to reach out for further information.
This compounded formulation of Zinc Oxide 12.5%/Lidocaine 5%/Pramoxine HCl 1% Topical/Rectal Gel is a semisolid preparation that is dispensed through a pump mechanism. This design allows for easy and precise application on the skin, ensuring targeted treatment or absorption of the active ingredients in a gel-like consistency. The formulation is indicated for the treatment of minor skin irritations, including cuts, scrapes, and burns, providing temporary relief from associated itching, burning, and discomfort. Furthermore, it can be used to soothe itching and burning associated with minor skin irritations due to poison ivy, poison oak, and poison sumac. However, it is important to note that this formulation should not be used on deep or puncture wounds, animal bites, or serious burns. If you have any questions regarding the use of this formulation, please do not hesitate to reach out.
This formulation is designed to provide targeted treatment for skin conditions or discomfort. The active ingredients work together to soothe, protect, and numb the affected area.
This formulation is dispensed through a pump mechanism, which allows for easy and precise application on the skin.
The formulation is a semisolid gel, which allows for targeted application and absorption of the active ingredients.
Yes, this formulation can be used both topically and rectally, depending on the specific needs of the patient.
Zinc Oxide is known for its protective and soothing properties. It forms a barrier on the skin, protecting it from irritants and promoting healing.
Lidocaine is a local anesthetic. It works by numbing the skin, providing relief from discomfort or pain.
Pramoxine HCl is also a local anesthetic. It works in conjunction with Lidocaine to provide additional numbing and pain relief.
The frequency of application will depend on the specific needs of the patient and the instructions of the healthcare provider. Always follow the directions provided by your healthcare provider.
As with any medication, there can be side effects. These may include skin irritation or allergic reactions. If you experience any unusual symptoms, contact your healthcare provider immediately.
Before using this formulation with other medications, it is important to discuss it with your healthcare provider to avoid any potential interactions.
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)
