Label: GREEN BEAUTY HAND SANITIZER- alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 December 6, 2022

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  • Drug Facts

  • Active ingredient

    Ethyl alcohol 70%

    Purpose

    Antiseptic

  • Uses

    to decreases bacteria on the skin that could cause disease

  • Warnings

    For external use only

    Flammable, Keep away from heat and flame.

    When using this product,

    keep out of eyes in case of contact with eyes, flush thoroughly with water, avoid contact with broken skin, do not inhale or ingest

    Stop use and ask a doctor if

    irritation or redness develops, condition persists for more than 72 hours

    Keep out of reach of children.

    If swallowed, get medical help or contact Poison Control Center right away.

  • Directions:

    wet hands thoroughly with product and allow to dry without wipping, for children under 6, use only under adult supervision, not recommended for infants

  • Other information:

    do nto store above 105°F may discolor some fabrics, harmful to wood finishes and plastic

  • Inactive Ingrediets:

    water, aloe barbadensis leaf juice, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, Fragrance. benzophennane-4, blue 1, yellow 5.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    GREEN BEAUTY HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79347-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERYL MONOCAPRYLOCAPRATE (UNII: G7515SW10N)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79347-000-013800 mL in 1 BOTTLE; Type 0: Not a Combination Product07/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/09/2020
    Labeler - GTP International Corp (118862131)
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