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Lexette Foam
  • Professionals
  • FDA PI

Lexette Foam

Generic name:halobetasol propionate
Dosage form: aerosol, foam
Drug class:Topical steroids

Medically reviewed by Drugs.com. Last updated on Jul 1, 2021.

Indications and Usage for Lexette Foam

LEXETTE® is indicated for the topical treatment of plaque psoriasis in patients 12 years of age and older.

Lexette Foam Dosage and Administration

Shake can prior to use. Apply LEXETTE as a thin uniform film to the affected skin twice daily for up to two weeks. Rub in gently. Wash hands after applying the product.

Discontinue therapy when control is achieved. If no improvement is seen within two weeks, reassessment of the diagnosis may be necessary.

Treatment beyond two weeks is not recommended and the total dosage should not exceed 50 grams per week because of the potential for the drug to suppress the hypothalamic-pituitary-adrenal (HPA) axis [see Warnings and Precautions (5.1)]. Do not use with occlusive dressings unless directed by a physician.

Avoid use on the face, groin, or axillae.

Avoid contact with eyes.

LEXETTE is for topical use only.

LEXETTE is not for ophthalmic, oral, or intravaginal use.

Dosage Forms and Strengths

LEXETTE® (halobetasol propionate) topical foam is a white to off-white topical foam. Each gram of LEXETTE, 0.05% contains 0.5 mg of halobetasol propionate.

Contraindications

None.

Warnings and Precautions

Hypothalamic-Pituitary-Adrenal (HPA) Axis Suppression and Other Adverse Endocrine Effects

LEXETTE is a topical corticosteroid that has been shown to suppress the hypothalamic-pituitary-adrenal (HPA) axis.

Systemic effects of topical corticosteroids may include reversible HPA axis suppression, with the potential for glucocorticosteroid insufficiency. This may occur during treatment or upon withdrawal of treatment of the topical corticosteroid. The p...