AWAKEN BY QUALITY CHOICE HAND SANITIZER CITRUS COCONUT (ETHYL ALCOHOL) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC]

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  • AWAKEN BY QUALITY CHOICE HAND SANITIZER CITRUS COCONUT (ETHYL ALCOHOL) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC]

AWAKEN BY QUALITY CHOICE HAND SANITIZER CITRUS COCONUT (ETHYL ALCOHOL) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC]
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NDC 63868-481-08
Set ID 20eb2d20-d414-431d-8c6b-febd72a28f29
Category HUMAN OTC DRUG LABEL
Packager Chain Drug Marketing Association Inc
Generic Name
Product Class
Product Number
Application Number PART333E
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  • Active ingredient

    Ethyl Alcohol 65%

    Purpose

    Antiseptic

  • Uses

    helps eliminate bacteria on hands.

  • Warnings

    For external use only.

    • Flammable.
    • Keep away from source of heat or fire.

    When using this product

    avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor if

    irritation or redness develops and lasts.

    Keep out of reach of children.

    In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

  • Directions

    Put enough product in your palm to cover hands and rub hands together until dry. Children under 6 years should be supervised when using this product.

  • Other information

    • store at a temperature below 110°F (43°C).
    • may discolor certain fabrics or surfaces.
  • Inactive ingredients

    Water (Aqua), Fragrance (Parfum), Carbomer, Glycerin, Isopropyl Myristate, Isopropyl Alcohol, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Mannitol, Cellulose, Tocopheryl Acetate, Hydroxypropyl Methylcellulose, PEG-60 Almond Glycerides, Chromium Hydroxide Green (CI 77289), Yellow 5 (CI 19140).

  • Questions or comments?

    1-284-449-9300

  • Label Copy

    Image of the label

  • INGREDIENTS AND APPEARANCE
    AWAKEN BY QUALITY CHOICE HAND SANITIZER  CITRUS COCONUT
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-481
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL650 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER 934 (UNII: Z135WT9208)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MANNITOL (UNII: 3OWL53L36A)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    PEG-60 ALMOND GLYCERIDES (UNII: 4Y0E651N0F)  
    CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63868-481-08259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/18/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/18/2016
    Labeler - Chain Drug Marketing Association Inc (011920774)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(63868-481)
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