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Tolnaftate by Premier Brands of America Inc.

Dosage form: aerosol, spray
Ingredients: TOLNAFTATE 1.3g in 130g
Labeler: Premier Brands of America Inc.
NDC Code: 56104-037

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.

PB Tolnaftate Jock Itch Powder Spray - Talc Free

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

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

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, if products get into eyes, rinse eyes thoroughly with water
  • 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

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 unless directed by a doctor.

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
  • if nozzle clogs, clean with a pin

Other information

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

Inactive ingredients

BHT, Isobutane, Kaolin, PPG-12-Buteth-16, SD Alcohol 40-B, Zea Mays (Corn) Starch

Questions?

call 1-866-964-0939

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Best Choice

MEDICATED 

Jock Itch Powder Spray

Tolnaftate 1%

  • Cures most jock itch 
  • Relieves itching, chafing and burning
  • Talc- Free

NET WT 4.6 OZ (130 g)

TOLNAFTATE 
tolnaftate jock itch powder spray - talc free aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56104-037
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 
KAOLIN 
PPG-12-BUTETH-16 
ALCOHOL 
ZEA MAYS SUBSP. MAYS WHOLE 
Packaging
#Item CodePackage Description
1NDC:56104-037-46130 g in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C10/31/2017
Labeler - Premier Brands of America Inc. (080051232)

 
Premier Brands of America Inc.

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Medically reviewed on Nov 10, 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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