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winter vanilla hand sanitizer (Wal-Mart Stores Inc)

Available Formats

Dosage Form Package Information Links
LIQUID 1 BOTTLE, PLASTIC in 1 PACKAGE (49035-109-02) > 30 mL in 1 BOTTLE, PLASTIC (49035-109-01) Label Information

Complete winter vanilla hand sanitizer Information

  • ACTIVE INGREDIENT

    Active ingredient         purpose

    Alcohol 75%              Antiseptic

    Uses For hand washing to decrease bacteria on the skin.

    Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

    Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

    Warnings

    For external use only.

    FLAMMABLE. Keep away from flame or high heat.

    When using this product

    Avoid contact with eyes. If contact occurs, flush eyes with water.

    Avoid contact with broken skin

    Directions

    Wet hands thoroughly with product and allow to dry without wiping.

    For children under 6, use only under adult supervision.

    Not recommended for infants.

    Inactive ingredients: Water (Aqua, Eau), Fragrance (Parfum), Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Ultramarines (CI 77007).

    May Contain: FD&C Red No. 4 (CI 14700), FD&C Yellow No. 5 (CI 19140), FD&C Blue No. 1 (CI 42090), D&C Red No. 33 (CI 17200).


  • PRINCIPAL DISPLAY PANEL

    carton

    bottle

    limited time only

    bodycology hand sanitizer

    1 Fl Oz. 30 mL


  • INGREDIENTS AND APPEARANCE
    WINTER VANILLA HAND SANITIZER  BODYCOLOGY
    alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-109
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75   in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GELATIN (UNII: 2G86QN327L)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ULTRAMARINE BLUE (UNII: I39WR998BI)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:49035-109-02 1 in 1 PACKAGE
    1 NDC:49035-109-01 30 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 05/22/2013
    Labeler - Wal-Mart Stores Inc (051957769)
    Registrant - Wal-Mart Stores Inc (051957769)
    Establishment
    Name Address ID/FEI Business Operations
    Landy International 545291775 manufacture(49035-109)