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Tolnafate by Chain Drug Consortium, LLC

Medically reviewed on December 5, 2017

Dosage form: aerosol, spray
Ingredients: TOLNAFTATE 1.3g in 130g
Labeler: Chain Drug Consortium, LLC
NDC Code: 68016-653

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.

Premier Value Tolnaftate Jock Itch Powder Spray

Active ingredient

Tolnaftate 1%



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

For external use only.


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.

  • 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


call 1-866-964-0939

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Premier Value


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 jock itch powder spray - talc free aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-653
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:68016-653-46130 g in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C10/31/2017
Labeler - Chain Drug Consortium, LLC (101668460)

Chain Drug Consortium, LLC

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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.