LIQUID ANTIFUNGAL TREATMENT- tolnaftate liquid

Liquid Antifungal Treatment by

Drug Labeling and Warnings

Liquid Antifungal Treatment by is a Otc medication manufactured, distributed, or labeled by Hudson Health LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​Active ingredient

Tolnaftate 1%

​Purpose

Antifungal

Uses

for the treatment of athlete’s foot (tinea pedis) and ringworm (tinea corporis)

for effective relief of itching, scaling, cracking, burning and redness.

Warnings

For external use only.

Flammable

keep away from fire or flame.

Do not use

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

When using this product

avoid contact with the eyes.

Stop use and consult a doctor if

• irritation occurs or if there is no improvement within 4 weeks

Keep out of reach of children.

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

​Directions

• wash the affected area and dry thoroughly.
• apply a thin layer of the product 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 spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.
• for athlete’s foot and ringworm, use daily for 4 weeks.
• if condition persists longer, consult a doctor.
• this product is not effective on the scalp or nails.

​Other information​

• Store at room temperature 15°-30°C (59° - 86°F)
• Keep tightly closed when not in use

​Inactive ingredient

Acetone, Water, Propylene Glycol, Tocopherol Acetate.

Questions?

Call 1-866-964-0939

Principal Display Panel

Comfort zone

liquid antifungal treatment

with vitamin e to moisturize

TOLNAFTATE 1%/ANTIFUNGAL

Maxiumum Strength

Brush- On Applicator

SHAKE WELL BEFORE USE

1 FL. OZ. (30 mL)

INGREDIENTS AND APPEARANCE

LIQUID ANTIFUNGAL TREATMENT 
tolnaftate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72446-012
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 mL

Inactive Ingredients
Ingredient Name	Strength
ACETONE (UNII: 1364PS73AF)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72446-012-01	1 in 1 CARTON	03/29/2024
1		30 mL in 1 BOTTLE, WITH APPLICATOR; 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	03/29/2024

Labeler - Hudson Health LLC (081276171)