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Anti-Fungal by Rij Pharmaceutical Corporation

Dosage form: powder
Ingredients: TOLNAFTATE .45g in 45g
Labeler: Rij Pharmaceutical Corporation
NDC Code: 53807-123

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Anti-Fungal Powder

Active Ingredient

Tolnaftate 1 %




  • for effective treatment of most athlete's foot (tinea pedis) and jock itch (tinea cruris)
  • relieves itching, scaling, burning, irritation and discomfort
  • clears up most athlete's foot infection and, with daily use, helps to keep it from coming back


For external use only

Do not use on children under 2 years of age.

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 (for athlete's foot) or within 2 weeks (for jock itch)

Keep out of reach of children.

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

  • shake well before use
  • clean 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
  • this product is not effective on the scalp or nails

For athletes foot

  • use daily for 4 weeks 
  • pay special attention to the spaces between the toes
  • wear well-fitting, ventilated shoes
  • change shoes and socks at least once a daily
  • to prevent athlete's foot: clean and dry feet thoroughly, apply once or twice daily

For jock itch

  • use daily for 2 weeks

Other information

store between 2° - 30° C (36° - 86° F)

Inactive ingredients

starch, talc

Package Label Display

tolnaftate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53807-123
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:53807-123-4545 g in 1 BOTTLE, DISPENSING
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C03/16/1999
Labeler - Rij Pharmaceutical Corporation (144679156)
Rij Pharmaceutical Corporation144679156manufacture(53807-123)

Rij Pharmaceutical Corporation

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Medically reviewed on Apr 30, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.