Cenovia label

Cenovia

Cenovia Recall

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Side Effects & Adverse Reactions

There is currently no warning information available for this product. We apologize for any inconvenience.

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

Uses

There is currently no usage information available for this product. We apologize for any inconvenience.

History

There is currently no drug history available for this drug.

Other Information

CENOVIA® is comprised of 2 g of Hydroquinone USP, 25 mg of Fluticasone Propionate USP, and 25 mg of Tretinoin USP for dermatological use.1 CENOVIA® also contains a Cream Base containing purified water, white petrolatum, sorbitol solution, cetearyl alcohol, propylene glycol, ceteareth-20, simethicone, glyceryl monostearate, polyethylene glycol monostearate, sorbic acid and BHT. When mixed as instructed, the final product provides a homogeneous cream mixture containing Hydroquinone, Fluticasone Propionate, Tretinoin comparable to the active ingredients (Alustra® 5%, Cutivate® 0.05%, and Retin-A® 0.05%) contained in CENOVIA®.2

1
Certificate of analysis on file
2
This product is not manufactured by Valeant Pharmaceuticals, manufacturer of Alustra® and Retin-A®, or by GlaxoSmithKline, manufacturer of Cutivate®.

Cenovia Manufacturers

  • Accumix Pharmaceuticals
    Cenovia | Accumix Pharmaceuticals
    No Recall

    Cenovia | Accumix Pharmaceuticals

    Cenovia | Accumix Pharmaceuticals

    The pharmacist must mix contents of each container with appropriate amount of Cream Base yielding a final volume of 50 grams at the time of dispensing. Pharmacist may utilize diluents if needed from the respective active component Material Safety Data Sheet only. For dermatological use only. This product should not be administered orally or into the eyes.