Label: PEANUTS HAND SANITIZER WITH ALOE- 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 September 19, 2020

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  • Active ingredient[s]

    Ethyl alcohol 63% VOL

  • Purpose

    Antiseptic

  • Uses

    • Hand Sanitizer to help reduce bacteria that potentially can cause disease.
    • For use when soap and water are not available.
  • Warnings

    • For external use only.
    • Flammable. Keep away from Heat or Flame.
  • DO NOT USE

    Do not use on children less than 12 months of age and on open skin wounds.

  • When using this product

    Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • Stop use and ask a doctor

    If irritation or rash occurs.

  • Keep out of reach of infants and children(It's not a toy).

    If swallowed, get medical help or contact a Poison Control Center immediately

  • Directions

    • Place enough product in your palm to completely cover your hands. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.

  • Other information

    Store at 5 C to 40 C (41 F to 104 F) May discolor some fabrics.

  • Inactive ingredients

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Fragrance, Maltodextrin, Glycerin, Propylene Glycol, Water.

  • PRINCIPAL DISPLAY PANEL

    image of front bottle label

    image of back bottle label

  • INGREDIENTS AND APPEARANCE
    PEANUTS HAND SANITIZER WITH ALOE 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76866-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL63 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76866-001-0159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/18/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/18/2020
    Labeler - 2 Market Llc (117072693)
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