Skip to Content

← See all Tolnaftate brands

Tolnaftate by Premier Brands of America Inc.

Medically reviewed on January 1, 2018

Dosage form: aerosol, powder
Ingredients: TOLNAFTATE 1.3g in 130g
Labeler: Premier Brands of America Inc.
NDC Code: 56104-527

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.

Medicated Jock Itch Powder Spray

Active ingredient

Tolnaftate 1%

​Purpose

Antifungal

Uses
  • cures most jock itch (tinea cruris)
  • relieves itching, burning and chafing associated with jock itch

​Warnings

For external use only.

Flammable:

Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120ºF.

​When using this product
  • do not get into eyes or mouth
  • use only as directed

Intentional misuse by deliberately concentrating and inhaling contents cans be harmful or fatal.

​Stop use and ask a doctor if
  • irritation occurs
  • no improvement 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. Do not use on children under 2 years of age. Do not use for diaper rash.

​Directions
  • wash affected area and dry thoroughly
  • shake can well and spray a thin layer over affected area twice daily (morning and night)
  • supervise children in the use of this product
  • use daily for 2 weeks; if conditions persist, consult a doctor
  • in case of clogging, clear nozzle under running water

​Other information

store between 20º and 30ºC (68ºF and 86º)

​Inactive ingredient

BHT, isobutane (propellent), PPG-12-buteth-16, SD alcohol 40-B (14%w/w), talc

​Questions?

Call 1-866-964-0939

Principal Display Panel

Premier

Medicated
Jock Itch
Powder Spray
Tolnaftate 1%

  • Cures and prevents most Jock Itch
  • Relieves itching and burning

NET WT 4.6 FL OZ (130g)

TOLNAFTATE 
medicated jock itch powder spray aerosol, powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56104-527
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (TOLNAFTATE) TOLNAFTATE1.3 g  in 130 g
Inactive Ingredients
Ingredient NameStrength
BUTYLATED HYDROXYTOLUENE 
ISOBUTANE 
PPG-12-BUTETH-16 
ALCOHOL 
TALC 
Packaging
#Item CodePackage Description
1NDC:56104-527-53130 g in 1 CANISTER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C01/01/2013
Labeler - Premier Brands of America Inc. (080051232)

 
Premier Brands of America Inc.

← See all Tolnaftate brands

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide