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Trichloroacetic Acid 35% Topical Solution is a liquid formulation designed for external application on the skin. This solution provides a targeted approach to skin treatment, delivering therapeutic agents directly to the affected area.
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.
Trichloroacetic Acid 35% Topical Solution is a compounded prescription medication designed for external application to the skin. This liquid formulation provides a convenient and versatile means of delivering medication, therapeutic agents, or other active ingredients for targeted treatment of various dermatological conditions or localized effects.
This medication is used to treat a variety of skin conditions, including Actinic Keratosis, Seborrheic Keratosis, Warts, Acne, and Melasma. It works by causing a controlled destruction of the outer layers of the skin, which helps to reduce the appearance of the affected areas.
Actinic Keratosis is a pre-cancerous skin condition caused by sun damage. Trichloroacetic Acid 35% Topical Solution can be used to reduce the appearance of Actinic Keratosis lesions, helping to improve the skin's appearance and health.
Seborrheic Keratosis is a benign skin condition characterized by the appearance of raised, waxy lesions. Trichloroacetic Acid 35% Topical Solution can be used to reduce the appearance of these lesions, providing relief and cosmetic improvement.
Warts, caused by a virus, can appear anywhere on the body. Trichloroacetic Acid 35% Topical Solution can be used to reduce the appearance of warts, aiding in their removal and reducing the risk of spread.
Acne, a common skin condition characterized by the appearance of pimples, blackheads, and whiteheads, can also be treated with Trichloroacetic Acid 35% Topical Solution. This medication can help reduce the appearance of acne lesions, leading to clearer skin.
Melasma, a skin condition characterized by the appearance of dark patches on the skin, can be effectively treated with Trichloroacetic Acid 35% Topical Solution. This medication can help reduce the appearance of Melasma lesions, improving skin tone and complexion.
Trichloroacetic Acid 35% Topical Solution is a appropriate treatment for Actinic Keratosis, Seborrheic Keratosis, Warts, Acne, and Melasma. Patients should follow their doctor's instructions for use and should contact their doctor if they have any questions or concerns. If you have any questions about Trichloroacetic Acid 35% Topical Solution, please reach out to your healthcare provider or pharmacist.
The Trichloroacetic Acid 35% Topical Solution is a liquid formulation specifically designed for external application to the skin. This solution is primarily used for the treatment of various dermatological conditions such as Actinic Keratosis, Seborrheic Keratosis, Warts, Acne, and Melasma. The medication works by causing a controlled destruction of the skin's outer layers, thereby reducing the appearance of lesions.
It is crucial to apply this solution as directed by a healthcare professional and only to the affected areas. It is not recommended for use on open wounds or on the face and other sensitive areas. Patients should also avoid sun exposure while using this medication as it can increase the risk of sunburn. Concurrent use of other topical medications should be avoided as it may increase the risk of skin irritation.
It is important to remember that the use of this medication should be under the guidance of a healthcare professional. If you have any questions or concerns about the use of Trichloroacetic Acid 35% Topical Solution, it is recommended to seek professional advice.
Trichloroacetic Acid 35% Topical Solution is a liquid formulation designed for external application to the skin. It is a versatile medication used to treat a range of dermatological conditions such as Actinic Keratosis, Seborrheic Keratosis, Warts, Acne, and Melasma. The solution works by causing a controlled destruction of the skin's outer layers, helping to reduce the appearance of the affected areas.
For Actinic Keratosis, the solution is applied directly to the affected area once or twice daily for up to three weeks. For Seborrheic Keratosis, Warts, Acne, and Melasma, the solution is applied once or twice daily for up to four weeks. It is important to note that the solution should not be used on open wounds, irritated or sunburned skin, or areas that have been treated with other topical medications. Avoid contact with the eyes, nose, and mouth. If contact occurs, rinse the area thoroughly with water.
Patients should be aware that Trichloroacetic Acid 35% Topical Solution may cause skin irritation, redness, burning, stinging, or itching. If these side effects occur, it is recommended to contact a healthcare provider. For any questions or concerns about Trichloroacetic Acid 35% Topical Solution or its use in treating Actinic Keratosis, Seborrheic Keratosis, Warts, Acne, or Melasma, please consult with a healthcare professional.
Trichloroacetic Acid 35% Topical Solution is a liquid formulation designed for external application to the skin. It is used to deliver medication, therapeutic agents, or other active ingredients for targeted treatment of various dermatological conditions or localized effects.
The purpose of this topical solution is to provide a convenient and versatile means of delivering medication or therapeutic agents to the skin. It is used for targeted treatment of various dermatological conditions or localized effects.
This solution is intended for external use only. Apply it to the affected area as directed by your healthcare provider. Do not use more or less of it or use it more often than prescribed by your doctor.
Do not apply this solution to broken skin or open wounds. Avoid contact with eyes, nose, mouth, and other sensitive areas. If the solution gets in these areas, rinse with plenty of water. Consult your healthcare provider if irritation or discomfort persists.
Side effects may include skin irritation, redness, burning, and peeling at the application site. If these side effects persist or worsen, contact your healthcare provider immediately.
Consult your healthcare provider before using this solution if you are pregnant, planning to become pregnant, or breastfeeding. The effects of this medication on an unborn baby or nursing infant are unknown.
Consult your healthcare provider before using this solution on children. The safety and effectiveness of this medication in children have not been established.
If you miss a dose, apply it as soon as you remember. However, if it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not apply a double dose to make up for a missed one.
Before starting any new skincare product, consult your healthcare provider. Some products may interact with this solution, causing skin irritation or other unwanted effects.
Store this solution at room temperature, away from heat and direct light. Do not freeze. Keep out of the reach of children and pets.
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)
