MAXIMUM STRENGTH ANTIFUNGAL LIQUID- tolnaftate liquid 
Chain Drug Marketing Association Inc

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Quality Choice Maximum Strength Antifungal Liquid

​Active ingredient

Tolnaftate 1% w/w

​Purpose

Antifungal

Uses

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

​Other information

​Inactive ingredient

Acetone, Water, Propylene Glycol, Tocopherol Acetate.

Questions?

Call 1-866-964-0939

Principal Display Panel

QC

Quality

Choice

Maximum Strength

Antifungal

Liquid

TOLNAFTATE 1%/ Antifungal

Quick-Drying Formula

With Vitamin E to Moisturize

Shake well before use

Maximum Strength

Brush-on Applicator

With the only active ingredient clinically proven

to cure and prevent athlete's foot

Treats fungus on toes, fingers & skin surrounding

and underneath the nails

Use brush for easy application

1 FL. OZ. (30 mL)

cartonlabel

MAXIMUM STRENGTH ANTIFUNGAL LIQUID 
tolnaftate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-301
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
TOCOPHEROL (UNII: R0ZB2556P8)  
ACETONE (UNII: 1364PS73AF)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-301-011 in 1 CARTON06/07/2024
130 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00506/07/2024
Labeler - Chain Drug Marketing Association Inc (011920774)

Revised: 6/2024
Document Id: 1a4f369a-52ee-dfb0-e063-6294a90a817b
Set id: 1a4f4d10-6782-ddb4-e063-6294a90ac206
Version: 1
Effective Time: 20240607
 
Chain Drug Marketing Association Inc