TINEA VERSICOLOR TREATMENT CREAM- clotrimazole cream

Tinea Versicolor Treatment Cream by

Drug Labeling and Warnings

Tinea Versicolor Treatment Cream by is a Otc medication manufactured, distributed, or labeled by Beautivity LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Clotrimazole 1%

PURPOSE

Antifungal

INDICATIONS & USAGE

Helps relieve & prevent itching, burning, cracking, and scaling associated with tinea nersicolor infections.

WARNINGS

For External Use Only

it on children under 2 years of age unless directed by a doctor.

avoid contact with eyes, if contact occurs, rinse the eyes very thoroughly with water.

Stop Using and Ask a Physician if irritation occurs or there is no improvement within 4 weeks.

keep out of the reach of young children.

DOSAGE & ADMINISTRATION

• Wash the affected area and dry thoroughly.
• Apply a thin layer over the affected area twice daily (morning and night), or as directed by a doctor, supervise children in the use of the product.
• If the condition persists longer, consult a doctor.

STORAGE AND HANDLING

Store at room temperature. Protect from excessive heat (above 104ºF/40ºC)

INACTIVE INGREDIENT

Purified Water, Camphor, Gentiana Lutea Root, Propylene Glycol, Glycerin, Methylparaben, Triethanolamine, Peppermint Oil

QUESTIONS

service@hermonhealth.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TINEA VERSICOLOR TREATMENT CREAM 
clotrimazole cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85398-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65)	CLOTRIMAZOLE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PEPPERMINT OIL (UNII: AV092KU4JH)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
METHYLPARABEN (UNII: A2I8C7HI9T)
GENTIANA LUTEA ROOT (UNII: S72O3284MS)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85398-002-01	60 g in 1 TUBE; Type 0: Not a Combination Product	05/12/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	05/12/2025

Labeler - Beautivity LLC (096573788)