TOLNAFTATE- antifungal liquid maximum strength liquid 
Target Corporation

----------

Target Tolnaftate 1% Anti-Fungal

​Active ingredient

Tolnaftate 1% w/w

​Purpose

Antifungal

Uses

Warnings

For external use only.

Do not use

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

When using this product

avoid contact with eyes.

Stop use and consult a doctor if

  • irritation occurs
  • there is no improvement in 4 weeks

Keep out of reach of children.

If accidental ingestion occurs, get medical help or contact a Poison Control Center right away.

​Directions

Read all warnings and directions. Use only as directed.

​Other information

​Inactive ingredient

Water, Acrylates Copolymer, Glycerin (RSPO), Phenoxyethanol, Tocopherol, Sodium Hydroxide, Ethylhexyglycerin

Questions?

Call 1-866-964-0939

Principal Display Panel

maximum

strength

antifungal

liquid

tolnaftate 1%

new formula

proven clinically effective in

the cure and prevention of

fungus on fingers, toes and

around nails

burning and scaling

relieves itching,

with moisturizer

easy to apply

applicator brush

NET 1 FL OZ (30 mL)

tolnaftate liquid tolnaftate label

TOLNAFTATE 
antifungal liquid maximum strength liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-091
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE0.3 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERIN (UNII: PDC6A3C0OX)  
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-091-0130 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product02/15/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00502/15/2021
Labeler - Target Corporation (006961700)

Revised: 2/2024
Document Id: 10a8fd7d-4a56-0282-e063-6394a90a07a9
Set id: b48e1f8f-fb74-366a-e053-2a95a90a22bf
Version: 5
Effective Time: 20240205
 
Target Corporation