Clobetasol Topical Solution 0.05pct Drug Medication Dosage Information
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Clobetasol: Topical solution (0.05%)

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Clobetasol 0.05% Topical Soln
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Clobetasol 0.05% Topical Soln
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Clobetasol 0.05% Topical Soln
Drug Image file default-drug-image.png
Clobetasol 0.05% Topical Soln

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 Clobetasol: Topical solution(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
Select a Medication

Clobetasol Propionate 0.05% Topical Solution

NDC: 604320133
  • 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
Store at room temperature (between 59 to 86 degrees F)
Protect from freezing
Clobetasol Propionate 0.05% Topical Solution

Reported Side Effects for Clobetasol Propionate 0.05% Topical Solution

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
Eye Irritation Incidence:
0.3%*
Severity: MILD
Onset: RAPID
Headache Incidence:
0.3%*
Severity: MILD
Onset: EARLY
Vesicular Rash Incidence:
0.3%*
Severity: MILD
Onset: DELAYED
Hair Loss Incidence:
0.3%*
Severity: MILD
Onset: DELAYED
Itching Incidence:
1.0-10.0%*
Severity: MILD
Onset: RAPID
Rash With Pustules Incidence:
1.0-10.0%*
Severity: MILD
Onset: EARLY
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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