HERMON JOCK ITCH SPRAY.- miconazole nitrate 2% liquid

Hermon Jock Itch spray. by

Drug Labeling and Warnings

Hermon Jock Itch spray. by is a Otc medication manufactured, distributed, or labeled by Beautivity LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Miconazole Nitrate 2%

PURPOSE

Antifungal

DOSAGE & ADMINISTRATION

• Cures most athlete's foot(tinea pedis), ringworm(tinea corporis) and jock itch(tinea cruris)
• Relieves itching, burning and scaling

WARNINGS

For external use only.

on children under 2 of age except under the advice and supervision of a doctor.

Avoid contact with the eye.

• Irritation occurs
• condition persists
• there is no improvement of athlete's foot or ringworm within 4 weeks or jock itch within 2 weeks.

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

INDICATIONS & USAGE

• Clean the affected area and dry thoroughly
• Shake well and spray a thin layer over affected area twice daily(morning and night) or as directed by a doctor
• Supervise children in the use of this product
• For athlete's foot, pay special attention to the spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
• For athlete's foot and righworm, use daily for 4 weeks
• For jock itch, use daily for 2 weeks
• This product is not effective on the scalp or nails

OTHER SAFETY INFORMATION

Store at room temperature 59°-86°F(15°-30°C).

INACTIVE INGREDIENT

Water, Alcohol, Propylene Glycol, Chlorhexidine Digluconate, Cnidium Monnieri Fruit Extract, Cortex Dictamni Root Extract, Kochia Scoparia Fruit Extract, Mentha Haplocalyx Leaf Extract, Sophora Flavescens Root Extract,Stemona Tuberosa Root Extract

QUESTIONS

service@hermohealth.com

Tel: 573-476-4179

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HERMON JOCK ITCH SPRAY. 
miconazole nitrate 2% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85398-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	1.2 g  in 60 g

Inactive Ingredients
Ingredient Name	Strength
DICTAMNUS DASYCARPUS ROOT BARK (UNII: LA97176ILS)
BASSIA SCOPARIA FRUIT (UNII: 04W97Z676Y)
MENTHA CANADENSIS FLOWERING TOP (UNII: 2492Y6JJNA)
CHLORHEXIDINE DIGLUCONATE (UNII: MOR84MUD8E)
CNIDIUM MONNIERI FRUIT OIL (UNII: JK0MS9P8YL)
ALCOHOL (UNII: 3K9958V90M)
STEMONA TUBEROSA ROOT (UNII: 7S9328671Z)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85398-030-01	1 in 1 CARTON	03/16/2026
1		60 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	03/16/2026

Labeler - Beautivity LLC (096573788)