Label: PEANUTS- 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 May 4, 2020

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  • Drug Facts

  • 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 in children less than 2 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 stop use and ask a doctor.

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

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

  • QUESTIONS

    Questions? 800-416-5651

  • Directions

    ■ Place enough product on hands to cover all surfaces. 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)

    Supervise children under 6 years old when using this to avoid swallowing.

  • Inactive ingredients

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Tocopherol, Water

  • Kills 99.99% Of Most Germs

    Distributed by 2Market, LLC

    © Peanuts

    www.peanuts.com

    Made in China

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    PEANUTS 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76866-003
    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
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76866-003-0158 mL in 1 BOTTLE; Type 0: Not a Combination Product04/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/30/2020
    Labeler - 2 Market Llc (117072693)
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