Olux Foam - Hydroalcoholic 0.05pct Drug Medication Dosage Information
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Olux: Foam - Hydroalcoholic (0.05%)

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Olux 0.05% Topical Foam
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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.

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
Usage By Strength
In-Depth Information
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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

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

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.

Third 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.

Lactation

Compatible - This drug is generally safe to take by nursing mothers.


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