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Hand Sanitizer (Wal-Mart Stores, Inc.)

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GEL 1 BOTTLE in 1 BOTTLE (49035-101-02) > 30 mL in 1 BOTTLE (49035-101-01) Label Information

Complete Hand Sanitizer Information

  • ACTIVE INGREDIENT

    Active Ingredient                             purpose

    Ethyl Alcohol 70%                          Antiseptic


    Uses: to decrease bacteria on the skin.

    Keep out of reach of children.

    Stop use and consult a doctor if irritation and redness develop and persist for more than 72 hours.

    Warnings: For external use only.
    Flammable. Keep away from heat and flame.
    When using this product: Avoid contact with eyes. If contact occurs, flush eyes with water. Avoid contact with broken skin.
    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

    Directions: Wet hands 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 (Aloe Vera leaf juice), Ultramarines (CI77007)
    May contain: FD C Red No.4(CI 14700, Aka504), FD C Yellow No. 5 (CI 19140,Ki4), FD C Blue No.1 (CI 42090, Ao1), D C Red No 33(CI 17200,Aka227)


    Image of bottle label
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  • PRINCIPAL DISPLAY PANEL

    Bodycology

    Hand Sanitizer


    30 mL 1 Fl Oz

    Image of tag label


  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER   BODYCOLOGY
    ethyl alcohol gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-101
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER INTERPOLYMER TYPE A (55000 MPA.S)) (UNII: 59TL3WG5CO)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GELATIN (UNII: 2G86QN327L)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    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:49035-101-02 1 in 1 BOTTLE
    1 NDC:49035-101-01 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333E 04/07/2011
    Labeler - Wal-Mart Stores, Inc. (051957769)