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VAGI-CURE (REGULAR STRENGTH) (SCI International, Inc. DBA Continental Pharmaceuticals)

Available Formats

Dosage Form Package Information Links
CREAM 21 g in 1 TUBE (76466-075-07) Label Information

Complete VAGI-CURE (REGULAR STRENGTH) Information

  • Directions:

    Apply liberally to affected area. If needed may be repeated three top four times daily. Children under (2) two years of age: Consult a physician.


  • Active ingredients:

    Aloe Vera Gel, Carbomer, Cetyl Alcohol, De-ionized Water, Disodium EDTA, Fragrance, Glycerol Monostearate, Isopropyl Myristate, Isopropyl Palmitate, Lanolin Anhydrous, Methylparaben, Mineral Oil, Peg 100 Stearate, propylene Glycol, Propylparaben, Vitamin E (tocopherol)


  • Warnings:

    FOR EXTERNAL USE ONLY. Avoid contact with eyes.

    Stop use and ask 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 use if you have an unusual or abnormal vaginal discharge except under the supervision of a physician. Do not apply over large areas of the body.

    Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


  • STORAGE AND HANDLING

    Store at 15 to 30C (49 to 85F)

    Manufactured for:
    Continental Pharmaceutical Inc.
    5904 Enterprise Court
    Frederick MD 21703
    Web: scimedic.com
    03-0096


  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel – Tube Label

    FAST REFIEF from everyday itch!

    ~Recommended By Women~

    Vagi-cure

    Anti-Itch Cream

    Advanced Sensitive Medicated Cream

    Principal Display Panel – Tube Label

  • INGREDIENTS AND APPEARANCE
    VAGI-CURE (REGULAR STRENGTH) 
    benzocaine, benzalkonium chloride cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:76466-075
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 50 mg  in 1 g
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE .13 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    LANOLIN (UNII: 7EV65EAW6H)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:76466-075-07 21 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2011
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 01/01/2011
    Labeler - SCI International, Inc. DBA Continental Pharmaceuticals (114220648)
    Establishment
    Name Address ID/FEI Business Operations
    NATURAL ESSENTIALS, INC. 947484713 MANUFACTURE(76466-075)