HERMON ANTIFUNGAL STICK- 1% clotrimazole stick

Hermon Antifungal Stick by

Drug Labeling and Warnings

Hermon Antifungal Stick 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

DOSAGE & ADMINISTRATION

• For the treatment of most athlete's foot (tinea pedis), jock itch (tineacruris), and ringworm (tinea corporis)
• Relieves itching, burning, cracking,scaling and discomfort associated with these conditions

WARNINGS

For external use only.

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

avoid contact with eyes.

if irritation occurs or if there is no improvement within 4 weeks(for athlete's foot and ringworm) or within 2 weeks (for jock itch).

lf swallowed,get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

• Clean the affected area and dry thoroughly.
• Apply a thin layer of this product over affected area twice daily(morning and night).
• Use daily for 2weeks for jock itch, 4 weeks for athlete'sfoot and ringworm.
• Supervise childrenin the use of this product.

For athlete's foot:

Pay special attentionto the spaces between toes; wearwell-fitting, ventilated shoes and change shoes and socks at least once daily

INACTIVE INGREDIENT

Propylene Glycol, Stearyl Alcohol, Cetyl Alcohol, Butylene Glycol, Glycerin,Hydrogenated Castor Oil, Talc, Zinc Oxide,Kaolin, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Aloe Yohjyu Matsu Ekisu, Menthol,Sodium Benzoate, Phenoxyethanol

OTHER SAFETY INFORMATION

Store at room temperature.Keep cap tightly closed when not in use

QUESTIONS

service@hermonhealth.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HERMON ANTIFUNGAL STICK 
1% clotrimazole stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85398-021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65)	CLOTRIMAZOLE	0.4 g  in 40 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALOE (UNII: V5VD430YW9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
KAOLIN (UNII: 24H4NWX5CO)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CETYL ALCOHOL (UNII: 936JST6JCN)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
ZINC OXIDE (UNII: SOI2LOH54Z)
TALC (UNII: 7SEV7J4R1U)
MENTHOL, (+)- (UNII: C6B1OE8P3W)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85398-021-01	40 g in 1 CARTON; Type 0: Not a Combination Product	01/15/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	01/15/2026

Labeler - Beautivity LLC (096573788)