HERMON ANTIFUNGAL SOAP. 4 PACKS- tolnaftate 1% soap

Hermon Antifungal Soap. 4 packs by

Drug Labeling and Warnings

Hermon Antifungal Soap. 4 packs 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 athlete's foot, jock itch, ringworm, and other skin irritations.

WARNINGS

For external use only.

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

avoide contact with eyes, lf contact occurs, rinse thoroughly with water.

irritation occurs there is no improvement within 2weeks.

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

INDICATIONS & USAGE

• Wash the affected area thoroughly and allow Hermon Antifungal Soap to sit for 1-2 minutes before rinsing.
• Dry the area completely after washing.
• Consistent use leads to better results.

INACTIVE INGREDIENT

Aqua (Water), Melaleuca Alternifolia (Tea Tree) Leaf Oil, Sorbitol, ElaeisGuineensis (Palm) Oil, Cocos Nucifera (Coconut) Oil, Olea Europaea(Olive) Fruit Oil, Propylene Glycol, Glycerin, Stearic Acid, Lauric Acid.Myristic Acid, Sodium Myristate, Sodium Glutamate, Sodium Hydroxide, Sodium Dodecylbenzene Sulfonate, Sulfur Thermal Water.Hamamelis Virginiana(Witch Hazel) Extract, Ceramide, Lavender

STORAGE AND HANDLING

Store at room temperature. Protect from excessive heat(above 104°F/40°C)

QUESTIONS

visit us at www.hermonhealth.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HERMON ANTIFUNGAL SOAP. 4 PACKS 
tolnaftate 1% soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85398-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	4.64 g  in 464 g

Inactive Ingredients
Ingredient Name	Strength
OLEA EUROPAEA (OLIVE) FRUIT OIL (UNII: 6UYK2W1W1E)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
LAURIC ACID (UNII: 1160N9NU9U)
STEARIC ACID (UNII: 4ELV7Z65AP)
MYRISTIC ACID (UNII: 0I3V7S25AW)
CERAMIDE 7 (UNII: 9O83X0C77V)
HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER (UNII: 8FP93ED6H2)
LAVENDER OIL (UNII: ZBP1YXW0H8)
GLYCERIN (UNII: PDC6A3C0OX)
SULFUR (UNII: 70FD1KFU70)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM MYRISTATE (UNII: 06BLC4V0IV)
AQUA (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
SODIUM GLUTAMATE (UNII: W81N5U6R6U)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
ELAEIS GUINEENSIS (PALM) OIL (UNII: 5QUO05548Z)
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85398-020-01	464 g in 1 CARTON; Type 0: Not a Combination Product	11/25/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	11/25/2025

Labeler - Beautivity LLC (096573788)

Registrant - Beautivity LLC (096573788)