Label: HAND SANITIZER PLUS ALOE VERA- ethyl 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 July 25, 2020

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  • ACTIVE INGREDIENT

    ETHYL ALCOHOL 65%

  • PURPOSE

    ANTIMICROBIAL

  • USE

    • HAND SANITIZER CAN HELP REDUCE BACTERIA ON THE SURFACE OF SKIN.
  • WARNINGS

    FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.

    FOR EXTERNAL USE ONLY.

    WHEN USING THIS PRODUCT DO NOT USE IN 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

    KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

  • DIRECTIONS

    • APPLY PRODUCT ALL OVER HANDS UNTIL DRY.
    • CHILDREN SHOULD BE SUPERVISED AT ALL TIMES WHEN USING THIS PRODUCT.
  • OTHER INFORMATION

    • STORE BELOW 110°F (43°C)
    • MAY DISCOLOR CERTAIN FABRICS OR SURFACES
  • INACTIVE INGREDIENTS

    Purified Water (Aqua), PEG-6, Glycerin, Tocopheryl Acetate (Vitamin E), Aloe Barbadensis (Aloe Vera) Leaf Juice, Acrylates/Vinyl Isodecanoate Crosspolymer, Fragrance (Parfum)

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Nature Love_Hand Sani Gel_65pct EtOH

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER  PLUS ALOE VERA
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78902-104
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78902-104-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product07/25/2020
    2NDC:78902-104-32946 mL in 1 BOTTLE; Type 0: Not a Combination Product07/25/2020
    3NDC:78902-104-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product07/25/2020
    4NDC:78902-104-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product07/25/2020
    5NDC:78902-104-06177 mL in 1 BOTTLE; Type 0: Not a Combination Product07/25/2020
    6NDC:78902-104-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product07/25/2020
    7NDC:78902-104-24739 mL in 1 BOTTLE; Type 0: Not a Combination Product07/25/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/25/2020
    Labeler - Jocott Brands, Inc. (080399826)
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