Label: UP AND UP JOCK ITCH RELIEF- clotrimazole cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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.

Drug Label Information

Updated July 8, 2016

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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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