Label: PERSONAL CARE HAND SANITIZER WITH MOISTURIZERS VITAMIN E- ethyl alcohol liquid

  • 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 April 6, 2018

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  • Active ingredient

    Ethyl Alcohol 62% v/v

  • Purpose

    Antimicrobial

  • Use

    hand sanitizer to help reduce bacteria on the skin

  • Warnings

    Flammable. Keep away from fire and flame. For external use only

  • When using this product

    ■ do not use i or near the eyes. In case of contact, rinse eyes thoroughly with water.

  • Stop use and ask a doctor if

    ■irritation or rash appears and lasts

  • Keep out of reach of children

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

  • Directions

    ■ place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry ■ children under 6 years of age should be supervised when using this product

  • Other infromation

    ■ store below 105ºF(41ºC) ■ may discolor certain fabrics or surfaces

  • Inactive ingredients

    water, aloe barbadensis leaf juice,carbomer, fragrance, glycerin, propylene glycol, tocopheryl acetate (vitamin E), triethanolamine

  • Package Label

    Package Label

  • INGREDIENTS AND APPEARANCE
    PERSONAL CARE  HAND SANITIZER WITH MOISTURIZERS VITAMIN E
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72133-051
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72133-051-08236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/05/2018
    2NDC:72133-051-12355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/05/2018
    3NDC:72133-051-0250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/05/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/05/2018
    Labeler - Delta Brands & Products LLC (080999173)
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