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Bencort Lotion
  • Professionals
  • FDA PI

Bencort Lotion

Generic name:benzoyl peroxide and hydrocortisone
Dosage form: lotion, kit
Drug class:Topical acne agents

Medically reviewed by Drugs.com. Last updated on Nov 22, 2021.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

INDICATIONS AND USAGE:

For the treatment of acne vulgaris.

Bencort Lotion Dosage and Administration

Shake well before use. Apply a thin film, 1 to
3 times daily, gently massaging into skin or as directed by a physician.

TO THE PHARMACIST

At the time of dispensing, add the contents of the
Bencort Benzoyl Peroxide Powder vial to the Bencort Lotion in the bottle.
Shake well to ensure uniform dispersion. Place expiration date of three (3) months on
the label. Bencort Lotion is 25 grams net weight.

Contraindications

Bencort Lotion is contraindicated in patients
hypersensitive to benzoyl peroxide, hydrocortisone, other corticosteroids or to any
ingredient contained in this product. Topical steroids are contraindicated in viral
diseases of the skin, such as varicella or vaccinia. Topical corticosteroids should not
be used in patients with markedly impaired circulation since skin ulceration has
occurred in these patients following use of the drugs.

Warnings and Precautions

Irritation including peeling, itching and/or redness
may occur, especially at the start of treatment. If any of these effects persist or worsen,
stop using and contact your doctor immediately. Smaller amounts of the drug may need to
be applied less often. Consult your doctor for instructions. For external use only. Keep away
from the eyes and mucous membranes. If severe irritation or swelling develops, discontinue
use and seek appropriate therapy.

Adverse Reactions

The most frequent adverse reactions to benzoyl peroxide
are irritation and contact dermatitis. Although 0.5% hydrocortisone is considered
safe, the following adverse reactions have been reported with topical corticosteroids,<