AVON HEXASHIELD ATHLETES FOOT CREAM- tolnaftate cream 
Tai Guk Pharm. Co., Ltd.

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AVON HeXashield Althlete's Foot Cream

Active Ingredient

Tolnaftate 1 %

Purpose

Antifungal

Uses

Warnings

For external use only.

When using this product

  • avoid contact with the eyes

Stop use and ask a doctor if :

  • irritation occurs
  • there is no improvement within 4 weeks

Do not use on children

  • under 2 years of age except under the advice and supervision of a doctor

Keep out of reach of children.

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

Directions

Other information

Inactive Ingredients

butylated hydroxytolune, ceteth-20, cetyl alcohol, methylparaben, mineral oil, propylparaben, sorbitan monostearate, stearyl alcohol, water

Questions or comments?

Call toll free 1-800-FOR-AVON

www.avon.com

Principal Display Panel

HeXasheild

Compare to the active ingredient in Tinactin®

Cures & Prevents Most Athlete's Foot

AVON

EFFECTIVE TREATMENT OF:

- ATHLETE'S FOOT - JOCK ITCH - RINGWORM

HeXashield

ATHLETE'S FOOT CREAM

TOLNAFTATE 1% ANTIFUNGAL CREAM

NET WT 1 oz (28 g)

 AVON ATHLETES FOOT CREAM_1

 AVON ATHLETES FOOT CREAM_DF

AVON HEXASHIELD ATHLETES FOOT  CREAM
tolnaftate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43136-104
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
WATER (UNII: 059QF0KO0R)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
CETETH-20 (UNII: I835H2IHHX)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
MINERAL OIL (UNII: T5L8T28FGP)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43136-104-011 in 1 CARTON07/31/2019
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00507/31/2019
Labeler - Tai Guk Pharm. Co., Ltd. (689060246)
Establishment
NameAddressID/FEIBusiness Operations
Tai Guk Pharma. Co., Ltd.689060246manufacture(43136-104)

Revised: 1/2025
Document Id: 2aabc954-bc49-e806-e063-6394a90a05dd
Set id: 8f2b6a09-8cb0-0d17-e053-2995a90aa07f
Version: 2
Effective Time: 20250101
 
Tai Guk Pharm. Co., Ltd.