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Bayview Pharmacy's Benzocaine 2%/Aluminum Chloride Hexahydrate 20%/Urea 10% Topical Solution is a liquid formulation designed for external application. This versatile solution combines three active ingredients to effectively treat a range of dermatological conditions such as hyperhidrosis, intertrigo, pruritus, dermatitis, and fungal infections.
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 Benzocaine 2%/Aluminum Chloride Hexahydrate 20%/Urea 10% Topical Solution is a specially compounded liquid formulation designed for external application to the skin. It is a versatile and convenient treatment option for a variety of dermatological conditions, including hyperhidrosis, intertrigo, pruritus, dermatitis, and fungal infections.
This unique formulation combines the properties of benzocaine, aluminum chloride hexahydrate, and urea to create a potent solution with antiperspirant, anti-inflammatory, and antifungal effects. The benzocaine component works to alleviate sweating and irritation, while the aluminum chloride hexahydrate serves to reduce inflammation and itching. The urea component is instrumental in inhibiting the growth of fungi and bacteria.
Bayview Pharmacy's Benzocaine 2%/Aluminum Chloride Hexahydrate 20%/Urea 10% Topical Solution is easy to apply and can be used daily to help manage symptoms and improve skin health. It provides targeted treatment for specific skin conditions, delivering the active ingredients directly to the affected area.
For any questions or concerns about this formulation or how it can help manage your specific condition, please do not hesitate to contact us. We are here to provide you with the necessary information and support to ensure the best possible outcome for your skin health.
This compounded formulation of Benzocaine 2%/Aluminum Chloride Hexahydrate 20%/Urea 10% Topical Solution is a liquid formulation designed for external application to the skin. It is a versatile treatment option for various dermatological conditions including hyperhidrosis, intertrigo, pruritus, dermatitis, and fungal infections. The active ingredients in this formulation work synergistically to provide targeted relief.
Benzocaine 2% serves as a local anesthetic, effectively reducing pain and itching associated with the aforementioned conditions. Aluminum Chloride Hexahydrate 20% acts as an astringent, helping to minimize sweating and inflammation. Urea 10% is a keratolytic agent that softens and removes the outer layer of the skin, enhancing the absorption of the other active ingredients.
While this formulation is generally well tolerated, some patients may experience skin irritation, burning, or stinging. It is recommended that patients apply the solution to the affected area no more than 3-4 times daily, avoiding contact with the eyes, nose, and mouth. If any adverse reactions occur, patients should discontinue use immediately and consult their healthcare provider.
Patients are also advised against using this formulation on broken or irritated skin. If any questions or concerns arise regarding the use of this topical solution, patients should not hesitate to contact their healthcare provider for further guidance.
Benzocaine 2%/Aluminum Chloride Hexahydrate 20%/Urea 10% Topical Solution is a compounded formulation designed for external application to the skin. This liquid formulation combines three active ingredients, each with a unique therapeutic effect, to provide targeted treatment for a range of dermatological conditions.
Benzocaine, a local anesthetic, is included in the formulation to alleviate pain and itching associated with various skin conditions. Aluminum Chloride Hexahydrate, an astringent, is incorporated to reduce sweating and inflammation. Urea, a potent moisturizer, is added to soften and hydrate the skin, enhancing the overall effectiveness of the formulation.
For hyperhidrosis, the solution works by constricting the sweat glands, thereby reducing excessive sweating. In the case of intertrigo, the solution helps to alleviate inflammation and itching, while also reducing the risk of infection. For pruritus and dermatitis, the solution provides relief from itching and inflammation, and helps to lower the risk of infection. For fungal infections, the solution aids in reducing inflammation, itching, and the risk of infection.
When using this formulation, it is crucial to adhere to the instructions provided by your healthcare provider. The solution should be applied directly to the affected area as directed. Avoid contact with the eyes, nose, and mouth. In case of accidental contact with the eyes, rinse thoroughly with water. If any irritation or redness occurs, discontinue use immediately and consult your healthcare provider.
If you have any queries about this formulation or its application, do not hesitate to reach out for further information. It is always important to understand the medication you are using and how it works to effectively manage your condition.
This is a liquid formulation intended for external application to the skin. It is designed to deliver medication, therapeutic agents, or other active ingredients for targeted treatment of various dermatological conditions or localized effects.
Apply the solution directly to the affected area of the skin as directed by your healthcare provider. Do not use more than the recommended dose without consulting your doctor.
The active ingredients in this solution are Benzocaine 2%, Aluminum Chloride Hexahydrate 20%, and Urea 10%.
Benzocaine is a local anesthetic. It helps to reduce pain or discomfort caused by minor skin irritations, sore throat, sunburn, teething pain, vaginal or rectal irritation, ingrown toenails, hemorrhoids, and many other sources of minor pain on a surface of the body.
Aluminum Chloride Hexahydrate is an astringent. An astringent shrinks or constricts body tissues and can be helpful in protein precipitation and disinfection.
Urea is used to treat dry/rough skin conditions (such as eczema, psoriasis, corns, callus) and some nail problems (e.g., ingrown nails). It can also help to remove dead tissue in some wounds to help wound healing.
Like all medicines, this topical solution can cause side effects, although not everybody gets them. Some common side effects include redness, mild stinging, or irritation at the application site. If you notice any severe or persistent side effects, please contact your healthcare provider immediately.
If you are pregnant or breastfeeding, it is important to consult your healthcare provider before using this solution to understand any potential risks or precautions.
Before using this solution on children, it is recommended to consult a healthcare provider. The safety and effectiveness of this solution in children may vary based on the condition and the child's age and overall health.
If you miss a dose, apply it as soon as you remember. If it is near the time of the next dose, skip the missed dose. Apply your next dose at the regular time. 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)
