Label: JOCK ITCH- tolnaftate spray

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated October 13, 2020

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  • Active ingredient

    Tolnaftate 1%

  • Purpose

    Antifungal

  • Uses

    cures most jock itch
    for effective relief of itching, chafing and burning
  • Warnings

    For external use only

    Flammable: Do not use while smoking or near heat or flame

    Do not use

    on children under 2 years of age unless directed by a doctor

    When using this product

    avoid contact with the eyes
    use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
    contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F (49°C).

    Stop use and ask a doctor if

    irritation occurs
    there is no improvement within 2 weeks

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

  • 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 condition persists longer, ask a doctor
    this product is not effective on the scalp or nails
    in case of clogging, clean nozzle with a pin
  • Other information

    store at 20-25°C (68-77°F)
  • Inactive ingredients

    alcohol denat., aluminum starch octenylsuccinate, isobutane, isopropyl myristate, propylene carbonate, sorbitan monooleate, stearalkonium hectorite, talc

  • Questions or comments?

    1-800-719-9260

  • Package/Label Principal Display Panel

    Compare to Tinactin® active ingredient

    Jock Itch Powder Spray

    TOLNAFTATE 1% / ANTIFUNGAL

    MAXIMUM STRENGTH

    Cures most jock itch

    Soothes & relieves itching, burning & chafing

    NET WT 4.6 OZ (130 g)

    jock itch image
  • INGREDIENTS AND APPEARANCE
    JOCK ITCH 
    tolnaftate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0695
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    ISOBUTANE (UNII: BXR49TP611)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
    STEARALKONIUM HECTORITE (UNII: OLX698AH5P)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    ColorWHITE (off-white) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0695-90130 g in 1 CAN; Type 0: Not a Combination Product06/08/2005
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333C06/08/2005
    Labeler - Walgreen Company (008965063)