Label: EQUATE VAGICAINE- 20% benzocaine and 3% resorcinol cream cream

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

Drug Label Information

Updated January 3, 2024

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  • Drug Facts

  • Active Ingredient 

    Benzocaine 20%

    Resorcinol 3%

  • Purpose

    External analgesic

    External analgesic

  • Uses

    Temporarily Relieves Itching

  • Warnings

    For external use only

    Allergy Allert

    Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other –caine anesthetics.

    Avoid contact with eyes

    in case of contact rinse thoroughly and immediately with water.

  • Stop use and ask if doctor if 

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

  • Keep out of the reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Adults and children 12 years and older

    Apply a finger tip amount (approxiamtely a 1 inch strip) to the affected areas not more than 3 to 4 times daily

    Children under 12 years

    ask a doctor

  • Other information 

    Questions?

  • Inactive ingredients 

    Water, Mineral Oil, Cetyl Alcohol, Propylene Glycol, Glyceryl Stearate, PEG-100 Stearate, Isopropyl Palmitate, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Retinyl Palmitate, Zea Mays (Corn) Oil, Cholecalciferol, Lanolin Alcohol, Fragrance, Methylparaben, Carbomer, Isopropyl Myristate, Isopropyl Stearate, Sodium Sulfite, Triethanolamine, Trisodium EDTA, Maltodextrin

  • Principal Dispaly panel Tube and Carton 

    Equate                NDC 79903-233-01Maxium Strength Vagicaine Anti itch Cream Benzocaine 20%, Resorcinol 3%NET WT 1OZ (28g)

    571010_Walmart_Vagicaine_Carton
    271010_Walmart_Vagicaine_Tube
  • INGREDIENTS AND APPEARANCE
    EQUATE VAGICAINE 
    20% benzocaine and 3% resorcinol cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-233
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE HYDROCHLORIDE (UNII: OG625Z9LEO) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE HYDROCHLORIDE200 mg  in 1 g
    RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL30 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    CORN OIL (UNII: 8470G57WFM)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ISOPROPYL STEARATE (UNII: 43253ZW1MZ)  
    SODIUM SULFITE (UNII: VTK01UQK3G)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    TETRASODIUM EDETATE DIHYDRATE (UNII: 3JGX4KKZ4A)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-233-011 in 1 CARTON12/01/2023
    128 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/01/2023
    Labeler - Walmart Inc. (051957769)
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