Label: TOLNAFTATE- jock itch powder aerosol, spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 2, 2024

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  • 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 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 persists, consult a doctor
    • if nozzle clogs, clean with a pin
  • ​Other information

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

  • ​Inactive ingredient

    BHT, isobutane, kaolin, PPG-12-buteth-16, SD alcohol 40-B, zea mays (corn) starch

  • Questions?

    Call 1-866-964-0939

  • Principal Display Panel

    Compare to the active

    ingredient, in Tinactin

    Jock Itch Powder Spray

    ANTIFUNGAL

    JOCK ITCH

    POWDER SPRAY

    tolnaftate 1%

    Cures most jock itch
    Relieves itching, chafing & burning
    Talc-free

    NET WT

    4.6 OZ (130 g)

    jock

  • INGREDIENTS AND APPEARANCE
    TOLNAFTATE 
    jock itch powder aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0782
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE1.3 g  in 130 g
    Inactive Ingredients
    Ingredient NameStrength
    KAOLIN (UNII: 24H4NWX5CO)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    ISOBUTANE (UNII: BXR49TP611)  
    PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
    ALCOHOL (UNII: 3K9958V90M)  
    ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-0782-4130 g in 1 CAN; Type 0: Not a Combination Product03/15/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00503/15/2021
    Labeler - Rite Aid Corporation (014578892)
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