Label: VAGICAINE MAXIMUM STRENGTH- benzocaine, resorcinol cream

  • NDC Code(s): 41250-142-64
  • Packager: Meijer Distribution Inc
  • Category: HUMAN OTC DRUG LABEL

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 February 28, 2019

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  • 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. Clean nozzle of tube by wiping thoroughly before replacing cap. Keep cap tightly closed between uses.

    children under 12 years

    ask a doctor
  • Other information

    store at 20-25°C (68-77°F)

  • Inactive ingredients

    aloe barbadensis leaf juice, carbomer homopolymer type C, cetyl alcohol, cholecalciferol, corn (zea mays) 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 anhydrous, tocopheryl acetate, trisodium HEDTA, trolamine

  • Questions or comments?

    1-800-719-9260

  • Principal Display Panel

    MAXIMUM STRENGTH

    vagicaine cream

    GYNECOLOGIST AND CLINICALLY TESTED

    Instant Long-Lasting Relief from Intense Itch

    Fast Acting – Relieves Painful Itching, Burning & Irritation on Contact

    Soothes with Viatmins E, A, & D + Aloe | Specifically Designed for the Vaginal Area

    Compare to Vagisil® active ingredients

    MAXIMUM STRENGTH

    vagicaine cream

    Pain Relieving Anti-Itch Cream

    NET WT. 1 OZ (28 g)

    Instant Relief

    vagicaine cream image
  • INGREDIENTS AND APPEARANCE
    VAGICAINE  MAXIMUM STRENGTH
    benzocaine, resorcinol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-142
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE20 g  in 100 g
    RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    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)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TRISODIUM HEDTA (UNII: K3E0U7O8KI)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41250-142-641 in 1 CARTON05/15/2009
    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 not finalpart34805/15/2009
    Labeler - Meijer Distribution Inc (006959555)
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