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Ketoprofen 10%/Ibuprofen 2.5% Topical Gel is a compounded medication, dispensed through a pump mechanism for easy and precise application. This semisolid formulation is designed for targeted treatment of conditions such as osteoarthritis, rheumatoid arthritis, tendinitis, bursitis, and fibromyalgia. The gel-like consistency allows for 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.
Ketoprofen 10%/Ibuprofen 2.5% Topical Gel is a specially compounded medication designed to address a range of musculoskeletal conditions. This unique formulation brings together two potent non-steroidal anti-inflammatory drugs (NSAIDs), ketoprofen and ibuprofen, to create a synergistic effect that effectively reduces inflammation and pain.
This topical gel is a semisolid formulation that is dispensed through a pump mechanism, facilitating easy and precise application on the skin. This allows for targeted treatment or absorption of the active ingredients directly into the affected area. The gel-like consistency ensures that the medication is absorbed through the skin, providing localized relief without systemic side effects.
It is crucial to note that Ketoprofen 10%/Ibuprofen 2.5% Topical Gel should not be applied to open wounds or areas of skin that are broken or irritated. Additionally, care should be taken to avoid contact with the eyes and mucous membranes. This is to prevent any potential irritation or adverse reactions.
Ketoprofen 10%/Ibuprofen 2.5% Topical Gel is a appropriate treatment option for a variety of musculoskeletal conditions. However, it is essential to follow the directions of your healthcare provider when using this medication. This will ensure the best possible outcome and minimize the risk of any potential side effects. If you have any questions or concerns about this formulation, please do not hesitate to reach out to your healthcare provider or pharmacist.
Ketoprofen 10%/Ibuprofen 2.5% Topical Gel is a semisolid formulation designed for targeted treatment of mild to moderate pain associated with musculoskeletal conditions such as arthritis, bursitis, and tendinitis.
The gel is dispensed through a pump mechanism, which allows for easy and precise application on the skin. It is recommended to apply the gel to the affected area no more than 4 times daily, gently massaging it until completely absorbed. It is important to wash hands after application to avoid accidental contact with eyes, nose, and mouth. If contact occurs, rinse thoroughly with water immediately.
Patients are advised to avoid applying the gel on open wounds or broken skin, and to refrain from using other topical medications on the same area. The use of heating pads, hot water bottles, or other sources of heat on the treated area should also be avoided.
If symptoms worsen or any adverse reactions are experienced, it is crucial to seek medical attention promptly. Prescribers should be aware that the combination of ketoprofen and ibuprofen may increase the risk of gastrointestinal bleeding and renal impairment. Therefore, careful monitoring of patients is recommended.
If you have any questions or concerns regarding the use of Ketoprofen 10%/Ibuprofen 2.5% Topical Gel, please do not hesitate to reach out for further information.
Ketoprofen 10%/Ibuprofen 2.5% Topical Gel is a compounded formulation that combines two potent nonsteroidal anti-inflammatory drugs (NSAIDs), Ketoprofen and Ibuprofen. This unique blend is designed to alleviate pain and inflammation, particularly in cases of mild to moderate musculoskeletal conditions such as arthritis, tendinitis, bursitis, and other joint and muscle pain.
The gel is dispensed through a pump mechanism, which allows for easy and precise application directly onto the skin of the affected area. The active ingredients are absorbed through the skin, targeting the site of pain and inflammation. The mechanism of action involves blocking the production of certain chemicals in the body that are responsible for causing inflammation and pain.
For optimal results, the gel should be massaged into the skin until it is completely absorbed. It is crucial to wash your hands thoroughly after applying the gel to avoid accidental contact with the eyes, nose, and mouth. The gel should not be applied to broken or irritated skin, and it is not recommended for use on the face or near the eyes.
As with any medication, it is essential to use Ketoprofen 10%/Ibuprofen 2.5% Topical Gel as directed by your healthcare provider. Always adhere to the instructions on the label and use the gel for the shortest duration necessary to manage your condition. If you have any questions or concerns about how to use this medication, it is recommended to consult with your healthcare provider for further guidance.
Ketoprofen 10%/Ibuprofen 2.5% Topical Gel is a compounded formulation that has demonstrated efficacy in managing a wide range of musculoskeletal conditions. These include osteoarthritis, rheumatoid arthritis, tendinitis, bursitis, and fibromyalgia. It has also been beneficial in treating muscle spasms, strains, and sprains. This formulation is particularly useful in reducing inflammation and pain associated with soft tissue injuries, including those resulting from sports activities. It has also shown effectiveness in alleviating post-operative pain and swelling.
It is important to note that this formulation should not be applied to open wounds or areas of the skin that are broken or irritated. It is designed for targeted treatment, facilitating easy and precise application on the skin for absorption of active ingredients in a gel-like consistency. This semisolid formulation is dispensed through a pump mechanism, ensuring a controlled and accurate dosage.
If you have any questions or concerns about the use of this formulation, it is recommended to consult with a healthcare professional. It is always important to use this medication as directed by a healthcare provider to ensure its safety and effectiveness.
This is a compounded formulation that contains 10% Ketoprofen and 2.5% Ibuprofen. It is a semisolid formulation that is dispensed through a pump mechanism for easy and precise application on the skin.
The gel works by delivering the active ingredients, Ketoprofen and Ibuprofen, directly to the targeted area for treatment or absorption. These ingredients are known for their anti-inflammatory and pain-relieving properties.
Apply 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 skin irritation, redness, or rash, stop using the product and contact your healthcare provider immediately.
Consult your healthcare provider before using this product if you are pregnant, planning to become pregnant, or breastfeeding.
Before starting any new medication, including this gel, inform your healthcare provider about all the medications you are currently taking to avoid any 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.
If you miss a dose, apply it as soon as you remember. However, if it is close to the time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.
The duration of treatment with this gel should be determined by your healthcare provider based on your specific condition and response to therapy.
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)
