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

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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.

In-Depth Information
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Olux 0.05% Topical Foam

NDC: 630320031
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




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

Storage Information
Do Not Store at Temperatures Above 120 degrees F (49 degrees C)
Store at controlled room temperature (between 68 and 77 degrees F)
Avoid excessive heat (above 104 degrees F)
Olux 0.05% Topical Foam

Reported Side Effects for Olux 0.05% Topical Foam

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
Drug-Induced Acne Incidence:
<2.0%*
Severity: MILD
Onset: DELAYED
Thinning Of Skin Incidence:
<2.0%*
Severity: SEVERE
Onset: DELAYED
Inflamed Hair Follicles Incidence:
<2.0%*
Severity: MILD
Onset: DELAYED
Unusual Skin Lightening Incidence:
<2.0%*
Severity: MILD
Onset: DELAYED
Infection Incidence:
<2.0%*
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
Dry Skin Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
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

Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.


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