HERMON ANTIFUNGAL .SOAP.- tolnaftate 1% soap

Hermon Antifungal .soap. by

Drug Labeling and Warnings

Hermon Antifungal .soap. 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

• For effective treatment of most athlete’s foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris).
• For effective relief of itching, burning and cracking skin.

INDICATIONS & USAGE

• Wash affected area well and let product sit 2–3 minutes before rinsing.
• Make sure to dry affected area thoroughly.
• 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.
• Use 1–2 times daily. Use daily for 4 weeks; if condition persists longer, ask a doctor.
• This product is not effective on the scalp or nails.

WARNINGS

For external use only.

on children under 2 years of age unless directed bya doctor.

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

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.

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

INACTIVE INGREDIENT

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

OTHER SAFETY INFORMATION

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

QUESTIONS

visit us at www.hermonhealth.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HERMON ANTIFUNGAL .SOAP. 
tolnaftate 1% soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85398-025
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
AQUA (UNII: 059QF0KO0R)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
SORBITOL (UNII: 506T60A25R)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
LAURIC ACID (UNII: 1160N9NU9U)
SODIUM GLUTAMATE (UNII: W81N5U6R6U)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
SUCROSE (UNII: C151H8M554)
SODIUM PALMITATE (UNII: JQ43KP6296)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85398-025-01	232 g in 1 CARTON; Type 0: Not a Combination Product	01/26/2026	01/30/2026
2	NDC: 85398-025-02	226 g in 1 CARTON; Type 0: Not a Combination Product	01/26/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	01/26/2026

Labeler - Beautivity LLC (096573788)