Olux: Foam - Hydroalcoholic (0.05%)

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Olux 0.05% Topical Foam

What is this Medicine?

CLOBETASOL (kloe BAY ta sol) is a corticosteroid. It is used on the skin to treat itching, redness, and swelling caused by some skin conditions.

Similar Generic Drugs : Clobetasol: Foam - Hydroalcoholic (0.05%)

CVS Pharmacy Patient Statistics for Olux: Foam - Hydroalcoholic(0.05%)

Generic vs. Brand Name Usage*

*Brand contains same active ingredient but may not represent FDA-approved generic equivalent

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Olux 0.05% Topical Foam

NDC: 400760031

Prescription Required
Not a Controlled Drug
(CSA Schedule)
FDA Approved

FDA approved for the following conditions:
Alopecia, Urticaria, Contact Dermatitis, Discoid Lupus Erythematosus, Eczema, Keloids, Rhus Dermatitis, Sarcoidosis, Pemphigus, Atopic Dermatitis, Lichen Planus, Granuloma Annulare, Pityriasis Rosea, Lichen Simplex, Psoriasis, Lichen Striatus, Exfoliative Dermatitis, Necrobiosis Lipoidica Diabeticorum

Storage Information
Do Not Store at Temperatures Above 120 degrees F (49 degrees C)
Flammable, keep away from heat and flame
Store at controlled room temperature (between 68 and 77 degrees F)

Olux 0.05% Topical Foam

Ingredients

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Reported Side Effects for Olux 0.05% Topical Foam

Drug-Induced Acne Incidence: <2.0%* Severity: MILD
Onset: DELAYED

Spider Veins Incidence: <2.0%* Severity: MILD
Onset: DELAYED

Striae Incidence: <2.0%* Severity: MILD
Onset: DELAYED

Sweat Rash Incidence: <2.0%* Severity: MILD
Onset: DELAYED

Ambras Syndrome Incidence: <2.0%* Severity: MILD
Onset: DELAYED

Unusual Skin Lightening Incidence: <2.0%* Severity: MILD
Onset: DELAYED

Inflamed Hair Follicles Incidence: <2.0%* Severity: MILD
Onset: DELAYED

Thinning Of Skin Incidence: <2.0%* Severity: SEVERE
Onset: DELAYED

Infection Incidence: <2.0%* Severity: MILD
Onset: DELAYED

Dry Skin Incidence: 1.0-10.0%* Severity: MILD
Onset: DELAYED

Rash With Pustules Incidence: 1.0-10.0%* Severity: MILD
Onset: EARLY

Itching Incidence: 1.0-10.0%* Severity: MILD
Onset: RAPID

Skin Redness Incidence: 1.0-10.0%* Severity: MODERATE
Onset: EARLY

Skin Irritation Incidence: 2.0-10.0%* Severity: MILD
Onset: EARLY

*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.

Pregnancy & Lactation Information

First Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

Second Trimester

Third Trimester