UP AND UP JOCK ITCH RELIEF (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]

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UP AND UP JOCK ITCH RELIEF (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]
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NDC 11673-504-58
Set ID f53d5418-5878-4c86-a2bb-b0ff61aec768
Category HUMAN OTC DRUG LABEL
Packager Target Corporation
Generic Name
Product Class Azole Antifungal
Product Number
Application Number PART333C
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  • Active ingredient

    Clotrimazole 1%

  • Purpose

    Antifungal

  • Uses

    •
    cures most jock itch
    •
    relieves itching, burning, scaling, chafing and discomfort which accompany this condition
  • Warnings

    For external use only

    Do not use

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

    When using this product

    avoid contact with the eyes

    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.

  • Directions

    •
    wash the affected area and dry thoroughly
    •
    apply 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
  • Other information

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

    benzyl alcohol, cetostearyl alcohol, cetyl esters wax, octyldodecanol, polysorbate 60, purified water, sorbitan monostearate

  • Questions?

    Call 1-888-547-7400

  • Package/Label Principal Display Panel

    Compare to active ingredient in Lotrimin®AF

    jock itch relief

    antifungal cream

    clotrimazole 1%

    cures most jock itch

    relieves itching, burning, scaling and chafing

    NET WT 0.5 OZ (14 g)

    Up & Up Jock Itch Relief image
  • INGREDIENTS AND APPEARANCE
    UP AND UP JOCK ITCH RELIEF 
    clotrimazole cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-504
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65) CLOTRIMAZOLE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ESTERS WAX (UNII: D072FFP9GU)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    WATER (UNII: 059QF0KO0R)  
    SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-504-581 in 1 CARTON09/17/2013
    114 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333C09/17/2013
    Labeler - Target Corporation (006961700)
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