HERMON JOCK ITCH ANTIFUNGAL TREATMENT .SOAP. BAR- tolnaftate 1% soap

Hermon Jock Itch Antifungal Treatment .Soap. Bar by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Tolnaftate 1%

PURPOSE

Antifungal

DOSAGE & ADMINISTRATION

Helps relieve and prevent itching, burning, cracking, and scaling associated with fungal infections such as jock itch, athlete's foot, ringworm, and other skin irritations.

WARNINGS

For external use only.

Avoid contact with the eye.

Stop and ask a doctor if irritation occurs or if there is no improvement within 2 weeks for jock itch or within 4 weeks for athlete's foot and ringworm.

Do not use on children under 2 years ofage unless directed by a doctor.

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

INDICATIONS & USAGE

• Wash affected area well and let product sit 2-3 minutes beforerinsing.
• Make sure to dry affected area thoroughly.
• Supervise children in theuse of this product.
• For Athlete's foot: pay special attention to the spacesbetween the toes; wear well-fitting, ventilated shoes and change shoes andsocks at least once daily.
• Use 1-2 times daily. Use daily for 4 weeks; if conditionpersists longer, ask a doctor.
• 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

Sucrose, Stearic Acid, Propylene Glycol, Sorbitol,Sodium Palmitate, Water, Glycerin, Butyrospermum Parkii (Shea) Butter,Lauric Acid, Sodium Hydroxide, Melaleuca Alternifolia (Tea Tree) Leaf Oil,Aloe Barbadensis Leaf Juice, Cocos Nucifera (Coconut) Oil, Fragrance

QUESTIONS

visit us at www.hermonhealth.com
Tel:573-476-4179

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HERMON JOCK ITCH ANTIFUNGAL TREATMENT .SOAP. BAR 
tolnaftate 1% soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85398-031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1.13 g  in 113 g

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
LAURIC ACID (UNII: 1160N9NU9U)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
WATER (UNII: 059QF0KO0R)
SODIUM PALMITATE (UNII: JQ43KP6296)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STEARIC ACID (UNII: 4ELV7Z65AP)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85398-031-01	113 g in 1 CARTON; Type 0: Not a Combination Product	01/01/2026
2	NDC: 85398-031-02	226 g in 1 CARTON; Type 0: Not a Combination Product	01/01/2026

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

Labeler - Beautivity LLC (096573788)