This topical cream formulation combines Cyclosporine A 2%, Ketoprofen 2.5%, and Phenylephrine HCl 0.1% to provide targeted relief for inflammatory skin conditions and localized pain. Cyclosporine A is an immunosuppressant that helps reduce inflammation, while Ketoprofen is a nonsteroidal anti-inflammatory drug (NSAID) that alleviates pain and swelling. Phenylephrine HCl acts as a vasoconstrictor to reduce redness and swelling. This semisolid preparation is dispensed in a pump mechanism.

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.
This compounded topical cream combines Cyclosporine A 2%, Ketoprofen 2.5%, and Phenylephrine HCl 0.1% in a semisolid preparation dispensed in a convenient pump mechanism. Designed for controlled and localized application on the skin, this formulation aims to deliver a synergistic effect by integrating the immunomodulatory, anti-inflammatory, and vasoconstrictive properties of its active ingredients.
Cyclosporine A is an immunosuppressive agent known for its ability to inhibit the activity of T-lymphocytes, essential components of the immune system. When applied topically, it can help reduce inflammation and alleviate symptoms associated with autoimmune and inflammatory skin conditions by modulating the immune response at the application site.
Ketoprofen is a nonsteroidal anti-inflammatory drug (NSAID) that provides analgesic and anti-inflammatory effects. By inhibiting the cyclooxygenase enzymes COX-1 and COX-2, Ketoprofen reduces the synthesis of prostaglandins, which are mediators of pain and inflammation. Its inclusion in the cream helps alleviate pain and reduce inflammation in affected areas.
Phenylephrine HCl is a selective alpha-1 adrenergic receptor agonist that causes vasoconstriction. Topically applied, it can decrease local blood flow, reducing redness and
Cyclosporine A 2%/Ketoprofen 2.5%/Phenylephrine HCl 0.1% Topical Cream is a compounded formulation designed for localized treatment and absorption of active ingredients through the skin. This formulation combines the immunosuppressive properties of Cyclosporine A, the anti-inflammatory effects of Ketoprofen, and the vasoconstrictive action of Phenylephrine HCl.
Cyclosporine A is a potent immunosuppressant that can interact with a wide range of medications. It is metabolized by the cytochrome P450 3A4 (CYP3A4) enzyme system, and concurrent use of drugs that inhibit or induce this enzyme can alter cyclosporine levels. Inhibitors of CYP3A4, such as ketoconazole, erythromycin, and grapefruit juice, can increase cyclosporine levels, potentially leading to toxicity. Conversely, inducers like rifampin and St. John's Wort can decrease cyclosporine levels, reducing its efficacy. Patients should be monitored for signs of cyclosporine toxicity, such as nephrotoxicity and hypertension, and dosage adjustments may be necessary.
Ketoprofen, a nonsteroidal anti-inflammatory drug (NSAID), can interact with other medications that affect renal function or increase the risk of gastrointestinal bleeding. Concurrent use with other NSAIDs, anticoagulants like warfarin, or antiplatelet agents such as aspirin can increase the risk of bleeding. Additionally, ketoprofen may reduce the antihypertensive effects of certain blood pressure medications, including ACE inhibitors and beta-blockers. Patients should be advised to report any signs of gastrointestinal bleeding, such as black or tarry stools, and to have their blood pressure monitored regularly.
Phenylephrine HCl is a sympathomimetic agent that can interact with other medications affecting the cardiovascular system. It may potentiate the effects of other vasoconstrictors and should be used cautiously in patients taking monoamine oxidase inhibitors (MAOIs) or tricyclic antidepressants, as these can enhance the pressor effects of phenylephrine. Patients with pre-existing cardiovascular conditions should be monitored for changes in blood pressure and heart rate.
It is crucial for both patients and prescribers to be aware of these potential interactions when considering the use of Cyclosporine A 2%/Ketoprofen 2.5%/Phenylephrine HCl 0.1% Topical Cream. A thorough review of the patient's current medication regimen and medical history is recommended to identify any potential risks. If you have any questions or concerns about this formulation or its interactions, please reach out to us for further guidance and support.
This topical cream formulation combines three active ingredients: Cyclosporine A, Ketoprofen, and Phenylephrine HCl, each contributing to the treatment of specific disease states through distinct mechanisms of action. The semisolid preparation is dispensed via a pump mechanism, ensuring a convenient and controlled application on the skin, which facilitates localized treatment and absorption of the active ingredients.
Cyclosporine A is an immunosuppressant that works by inhibiting the activity of calcineurin, a protein phosphatase involved in the activation of T-cells. By suppressing the immune response, Cyclosporine A helps reduce inflammation. Its topical application allows for targeted action at the site of inflammation, minimizing systemic exposure and potential side effects associated with oral administration.
Ketoprofen is a nonsteroidal anti-inflammatory drug (NSAID) that provides relief from pain and inflammation by inhibiting the cyclooxygenase (COX) enzymes, which are responsible for the synthesis of prostaglandins. Prostaglandins are lipid compounds that mediate inflammation and pain. By reducing their production, Ketoprofen alleviates symptoms associated with conditions like arthritis, musculoskeletal pain, and other inflammatory disorders. The topical delivery of Ketoprofen ensures that the drug acts directly at the site of pain.
Phenylephrine HCl is a sympathomimetic agent that primarily acts as a selective alpha-1 adrenergic receptor agonist. Its vasoconstrictive properties help reduce swelling and congestion by constricting blood vessels in the affected area. This action is beneficial in conditions where localized vasodilation contributes to symptoms, such as in certain dermatological conditions where reducing redness and edema is desired. The inclusion of Phenylephrine HCl in this formulation enhances the overall therapeutic effect by addressing vascular components of inflammation and discomfort.
The combination of these three active ingredients in a single topical cream provides a multifaceted approach to managing inflammatory and painful skin conditions. By delivering the medication directly to the affected area, the formulation maximizes therapeutic efficacy while minimizing systemic exposure and potential side effects. This targeted approach is particularly advantageous for patients who require localized treatment without the complications associated with systemic drug administration.
For prescribers, this formulation offers a versatile treatment option that can be tailored to the specific needs of patients with inflammatory skin conditions, musculoskeletal pain, or other localized issues. The pump mechanism ensures precise dosing and ease of use, promoting adherence to treatment regimens. Patients benefit from the convenience and effectiveness of a topical therapy that addresses multiple aspects of their condition.
If you have any questions or need further information about this formulation, please reach out to us at Bayview Pharmacy. Our team of compounding pharmacists is here to assist you with any inquiries or concerns you may have.
Cyclosporine A is an immunosuppressant that helps reduce inflammation and modulate the immune response in the skin, making it useful for treating conditions like psoriasis or eczema.
Ketoprofen is a nonsteroidal anti-inflammatory drug (NSAID) that helps alleviate pain and reduce inflammation in the affected area when applied topically.
Phenylephrine HCl is a vasoconstrictor that helps reduce redness and swelling by narrowing the blood vessels in the skin.
Dispense the cream using the pump mechanism and apply a thin layer to the affected area. Gently rub it in until fully absorbed. Follow your healthcare provider's instructions regarding the frequency and amount of application.
It is generally advised to avoid applying the cream on broken or severely irritated skin unless directed by a healthcare professional, as it may cause further irritation or adverse effects.
Possible side effects may include skin irritation, redness, or itching at the application site. If you experience severe reactions or symptoms persist, consult your healthcare provider.
While the cream is designed for topical use, individuals with sensitive skin should use it cautiously and consult a healthcare provider if they have concerns about potential reactions.
Store the cream at room temperature, away from direct sunlight and moisture. Keep it out of reach of children and pets.
Before using this cream with other topical medications, consult your healthcare provider to avoid potential interactions or reduced effectiveness of the treatments.
The time to see results can vary depending on the condition being treated and individual response. Some users may notice improvement within a few days, while others may require several weeks of consistent use.
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.
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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)