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Up and up vagicaine (Target Corporation)

Available Formats

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CREAM 1 TUBE in 1 CARTON (11673-142-64) > 28 g in 1 TUBE Label Information

Complete Up and up vagicaine Information

  • Active ingredients

    Benzocaine 20%

    Resorcinol 3%


  • Purpose

    External analgesic


  • Use

    temporarily relieves itching


  • Warnings

    For external use only

    When using this product

    avoid contact with the eyes

    Stop use and ask a doctor if

    condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

    Do not apply

    over large areas of the body

    Keep out of reach of children.

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


  • Directions

    adults and children 12 years and older

    apply a fingertip amount (approximately

    1-inch strip) to the affected area not more than 3 to 4 times daily

    children under 12 years

    ask a doctor


  • Other information

    store at 20°-25°C (68°-77°F)


  • Inactive ingredients

    aloe barbadensis leaf extract, carbomer homopolymer, cetyl alcohol, cholecalciferol, corn oil, fragrance, glyceryl monostearate, isopropyl myristate, isopropyl palmitate, isopropyl stearate, lanolin alcohol, methylparaben, mineral oil, PEG-100 stearate, propylene glycol, purified water, retinyl palmitate, sodium sulfite, tocopheryl acetate, trisodium HEDTA, trolamine


  • Questions?

    Call 1-888-547-7400


  • Principal Display Panel

    maximum strength

    vagicaine anti-itch cream

    benzocaine 20%/resorcinol 3%

    Compare to active ingredients in Vagisil® Maximum Strength

    NET WT 1 OZ (28 g)

    pain relieving cream

    instant long-lasting relief from intense itch associated with:

    antibiotics, discharge, imbalance in pH, irritating vaginal conditions

    Up & Up Vagicaine Image 1
    Up & Up Vagicaine Image 2

  • INGREDIENTS AND APPEARANCE
    UP AND UP VAGICAINE 
    benzocaine, resorcinol cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-142
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 20 g  in 100 g
    RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL 3 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    CORN OIL (UNII: 8470G57WFM)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    ISOPROPYL STEARATE (UNII: 43253ZW1MZ)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    SODIUM SULFITE (UNII: VTK01UQK3G)  
    TRISODIUM HEDTA (UNII: K3E0U7O8KI)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-142-64 1 in 1 CARTON
    1 28 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 08/25/2009
    Labeler - Target Corporation (006961700)