HERMON ANTIFUNGAL CLEANSING BAR- tolnaftate 1% soap

Hermon Antifungal Cleansing Bar by

Drug Labeling and Warnings

Hermon Antifungal Cleansing 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

• 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.

WARNINGS

For external use only

When using this product Avoid contactwith 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 of age except under the advice and supervision of 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.
• Supervisechildren 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 timesdaily. Use daily for 4 weeks; if condition persists longer, ask a doctor.
• This product is not effective on the scalp or nails.

OTHER SAFETY INFORMATION

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

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 LeafJuice, Cocos Nucifera (Coconut) Oil, Fragrance

QUESTIONS

Visit us at www.hermonhealth.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HERMON ANTIFUNGAL CLEANSING BAR 
tolnaftate 1% soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85398-029
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	4.52 g  in 452 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85398-029-01	452 g in 1 CARTON; Type 0: Not a Combination Product	02/02/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	02/02/2026

Labeler - Beautivity LLC (096573788)