MAXIMUM STRENGTH ANTIFUNGAL LIQUID- tolnaftate liquid

Maximum Strength Antifungal Liquid by

Drug Labeling and Warnings

Maximum Strength Antifungal Liquid by is a Otc medication manufactured, distributed, or labeled by Premier Brands of America Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​Active ingredient

Tolnaftate 1% w/w

​Purpose

Antifungal

Uses

• For the treament of athlete's foot (tinea pedis) and ring worm (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 in 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 the 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 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

premier solutions

MAXIMUM STRENGTH

ANTIFUNGAL

LIQUID

TOLNAFTATE 1%/ANTIFUNGAL

SHAKE WELL BEFORE USE

Maximum strength

Cures & prevents athlete's foot

Brush-on applicator

Treats fungus on skin & under the nails

1.0 FL OZ (30 mL)

INGREDIENTS AND APPEARANCE

MAXIMUM STRENGTH ANTIFUNGAL LIQUID 
tolnaftate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56104-900
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
WATER (UNII: 059QF0KO0R)
TOCOPHEROL (UNII: R0ZB2556P8)
ACETONE (UNII: 1364PS73AF)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56104-900-30	1 in 1 CARTON	01/02/2023
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	01/02/2023

Labeler - Premier Brands of America Inc. (063849780)