SANITIZER HAND SANITIZER (ETHYL ALCOHOL) LIQUID [AMERICAN SALES]

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SANITIZER HAND SANITIZER (ETHYL ALCOHOL) LIQUID [AMERICAN SALES]
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NDC 41520-235-01
Set ID 8bb4b9ad-4904-4885-a887-243f0e63bdb8
Category HUMAN OTC DRUG LABEL
Packager AMERICAN SALES
Generic Name
Product Class
Product Number
Application Number PART333E
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  • ACTIVE INGREDIENT

    ETHYL ALCOHOL 62 PERCENT

  • PURPOSE

    ANTIMICROBIAL

  • USES

    TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE.

  • WARNINGS

    FOR EXTERNAL USE ONLY.  FLAMMABLE KEEP AWAY FROM FIRE OR FLAME.

    WHEN USING THIS PRODUCT

    AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER.

    STOP USING THIS PRODUCT AND ASK DOCTOR IF

    IRRITATION OR RASH 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

    SPRAY ENOUGH PRODUCT IN YOUR PALM TO THOROUGHLY COVER YOUR HANDS.

    RUB HANDS TOGETHER BRISKLY UNTIL DRY.

    CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

  • OTHER INFORMATION

    STORE AT A TEMPERATURE BELOW 110 DEGREES FAHRENHEIT (43 DEGREES CELSIUS).

  • INACTIVE INGREDIENTS

    WATER, PROPYLENE GLYCOL, GLYCERIN, FRAGRANCE, ISOPROPYL MYRISTATE, TOCOPHERYL ACETATE, ALOE BARBADENSIS LEAF EXTRACT.

  • PRINCIPAL DISPLAY PANEL

    IMAGE OF HAND SANITIZER

  • INGREDIENTS AND APPEARANCE
    SANITIZER  HAND SANITIZER
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41520-235
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41520-235-017.4 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/06/2011
    Labeler - AMERICAN SALES (809183973)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOLLO HEALTH AND BEAUTY CARE201901209manufacture
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