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Tolnaftate by VALU MERCHANDISERS, CO

Dosage form: aerosol, spray
Ingredients: TOLNAFTATE 1.3g in 130g
Labeler: VALU MERCHANDISERS, CO
NDC Code: 63941-548

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.

Jock Itch Powder Spray

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

​Uses
  • cures most jock itch (tinea cruris)
  • relieves itch, 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. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

​When using this product
  • avoid contact with eyes
  • use only as directed

​Stop use and ask a doctor if
  • irritation occurs
  • no improvement within 2 weeks

​Do not use
  • on children under 2 years of age unless directed by a doctor.

​Keep out of reach of children.

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

​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 1-888-423-0139

​Principal Display Panel

Best Choice

Medicated

Jock Itch Powder Spray

Tolnaftate 1%

  • Cures most Symptoms or jock itch
  • relieves itching, chafing, and burning

Net WT 4.6 OZ (130 g)

TOLNAFTATE 
jock itch powder aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63941-548
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:63941-548-46130 g in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C12/11/2017
Labeler - VALU MERCHANDISERS, CO (868703513)

 
VALU MERCHANDISERS, CO

← See all Tolnaftate brands

Medically reviewed on Dec 11, 2017

Further information

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

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