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Ketoprofen 5%/Lidocaine 0.5% Topical Gel is a semisolid formulation, dispensed through a pump mechanism for easy and precise application. This compounded medication is designed for targeted treatment of conditions such as osteoarthritis, rheumatoid arthritis, tendinitis, bursitis, and neuropathic pain. The gel-like consistency allows for effective 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.
Ketoprofen 5%/Lidocaine 0.5% Topical Gel is a specially compounded medication designed to address a range of musculoskeletal conditions. These include osteoarthritis, rheumatoid arthritis, tendinitis, bursitis, and neuropathic pain. The formulation combines the potent anti-inflammatory properties of ketoprofen, a non-steroidal anti-inflammatory drug (NSAID), with the analgesic effects of lidocaine, a local anesthetic. Together, these active ingredients work synergistically to reduce inflammation and block nerve signals, thereby alleviating pain.
This topical gel is a semisolid formulation that is dispensed through a pump mechanism. This design facilitates easy and precise application on the skin, allowing for targeted treatment and efficient absorption of the active ingredients. By applying the gel directly to the affected area, patients can experience relief where it is most needed.
Generally, Ketoprofen 5%/Lidocaine 0.5% Topical Gel is well tolerated by most patients, with minimal side effects. Some individuals may experience skin irritation, itching, or redness at the application site. It is advised to avoid contact with the eyes and mucous membranes when using this medication.
It is intended to be used as part of a comprehensive treatment plan.
If you have any questions about this formulation or how it can be used to manage your condition, please do not hesitate to reach out to us. We are here to provide you with the information and support you need to make informed decisions about your health.
Ketoprofen 5%/Lidocaine 0.5% Topical Gel is a semisolid formulation designed for targeted treatment of conditions such as Osteoarthritis, Rheumatoid Arthritis, Tendinitis, Bursitis, and Neuropathic Pain. This unique formulation combines the anti-inflammatory properties of a non-steroidal anti-inflammatory drug (NSAID) with the local pain relief provided by an anesthetic. It is dispensed through a pump mechanism, which allows for easy and precise application on the skin.
It is important to note that this topical gel should not be applied to open wounds or broken skin. After application, patients should wash their hands thoroughly and avoid touching their eyes, nose, and mouth. Additionally, patients should be cautious about excessive sun exposure and are advised to use sunscreen when outdoors.
Patients should be aware that Ketoprofen 5%/Lidocaine 0.5% Topical Gel may interact with other medications, including other topical treatments, oral medications, and supplements. Therefore, it is crucial to inform your healthcare provider of all medications and supplements you are currently taking before starting this treatment. It is also recommended to avoid alcohol consumption while using this product.
While generally well-tolerated, some patients may experience side effects such as skin irritation, redness, itching, burning, or stinging. If any of these side effects occur, it is advised to stop using the product and contact your healthcare provider immediately.
If you have any further questions or concerns about Ketoprofen 5%/Lidocaine 0.5% Topical Gel or its potential interactions, please do not hesitate to contact us at Bayview Pharmacy.
Ketoprofen 5%/Lidocaine 0.5% Topical Gel is a compounded formulation that combines the therapeutic benefits of two potent medications, ketoprofen and lidocaine. This topical gel is designed to provide targeted relief from a variety of painful conditions by delivering the active ingredients directly to the affected area.
Ketoprofen, a non-steroidal anti-inflammatory drug (NSAID), works by inhibiting the production of certain chemicals in the body that trigger inflammation and pain. On the other hand, lidocaine, a local anesthetic, functions by blocking nerve signals in the area where the gel is applied. The synergistic action of these two medications helps to alleviate pain and reduce inflammation effectively.
This topical gel is particularly beneficial for managing pain associated with conditions such as osteoarthritis, rheumatoid arthritis, tendinitis, bursitis, and neuropathic pain. Osteoarthritis, a degenerative joint disease, and rheumatoid arthritis, an autoimmune disorder, both result in joint pain and stiffness. Tendinitis and bursitis are conditions characterized by inflammation of the tendons and bursae, respectively. Neuropathic pain, a type of chronic pain, is caused by nerve damage.
The Ketoprofen 5%/Lidocaine 0.5% Topical Gel is dispensed through a pump mechanism, which allows for easy and precise application. The gel is absorbed through the skin, delivering the active ingredients directly to the source of pain and inflammation. It is crucial to adhere to the usage instructions provided on the package and avoid applying more than the recommended amount. For any queries or concerns regarding the use of this medication, it is advisable to consult a healthcare professional.
This is a compounded formulation that contains Ketoprofen, a nonsteroidal anti-inflammatory drug (NSAID), and Lidocaine, a local anesthetic. It is designed to be applied topically to the skin for targeted treatment.
The formulation is dispensed through a pump mechanism, which allows for easy and precise application on the skin.
The gel has a semisolid consistency, which facilitates its application and absorption into the skin.
Ketoprofen works by reducing hormones that cause inflammation and pain in the body. Lidocaine works by blocking nerve signals in your body, thus reducing pain or discomfort caused by skin irritations.
Apply a thin layer of the gel to the affected area as directed by your healthcare provider. The pump mechanism allows for easy and precise application.
This gel is intended for external use only. Avoid contact with eyes, mouth, and other mucous membranes. If you are unsure about where to apply the gel, consult your healthcare provider.
If you experience any side effects such as redness, itching, or rash, stop using the product and contact your healthcare provider immediately.
If you are pregnant or breastfeeding, consult your healthcare provider before using this product. The effects of this gel on unborn babies or nursing infants are not known.
Before using this gel, inform your healthcare provider about any other medications you are currently taking to avoid potential drug interactions.
Store this gel at room temperature, away from heat and direct light. Do not freeze. Keep out of 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)
