Label: BODYCOLOGY HAND SANITIZER GIFT SET- ethyl alcohol gel

  • 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 August 16, 2010

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  • OVERDOSAGE

    Active Ingredients                  Purpose

    Ethyl Alcohol 70%                  Antiseptic

  • WARNINGS

    Warnings:

    -For external use only.

    -Flammable. Keep away from heat and flame.

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

  • PURPOSE

    Uses: to decrease bacteria on the skin
  • KEEP OUT OF REACH OF CHILDREN

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

  • INDICATIONS & USAGE

    When using this product avoid contact with eyes. If contact occurs, flush eyes with water. Avoid contact with broken skin.

  • DOSAGE & ADMINISTRATION

    Directions: wet hands with product and allow to dry without whiping. For children under 6, use only under adult supervision. Not recommended for infants.

  • INACTIVE INGREDIENT

    Inactive Ingredient: Water (Aqua/Eau), Fragrance (Parfum), Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis (Aloe Vera). May Contain: Ultramarines (CI 77007), Red 4 (CI 14700), Yellow 5 (CI 19140), Yellow 6 (CI 15985), Blue 1 (CI 42090), Red 33 (CI 17200), Ext. Violet (CI 60730, Green 3 (CI 42053)

    image of back label

  • PRINCIPAL DISPLAY PANEL

    Bodycology
    Hand Sanitizer Gift Set (Fragrances Include: brown sugar vanilla, cherry blossom, cucumber melon, midnight garden, sweet petals, white gardenia
    6 x 55 ml 1.86 oz
    image of front label

  • INGREDIENTS AND APPEARANCE
    BODYCOLOGY  HAND SANITIZER GIFT SET
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51706-400
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51706-400-026 in 1 KIT
    1NDC:51706-400-0155 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33308/13/2010
    Labeler - Landy International (545291775)
    Registrant - Wal-Mart Stores, Inc. (051957769)
    Establishment
    NameAddressID/FEIBusiness Operations
    Landy International545291775manufacture
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