Label: PEANNUTS HAND SANITIZER- alcohol liquid

  • NDC Code(s): 74274-120-01
  • Packager: Huizhou Bliss Commodity Co., Ltd
  • 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 3, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 68%

  • Purpose

     Antiseptic

  • Uses

    • To decrease bacteria on the skin that could cause disease.
    • Recommended for repeated use.
  • KEEP OUT OF REACH OF CHILDREN

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

  • warnings:

    • Flamable, keep away from heat and flame
    • For external use only.
    • Discontinue if skin away from heat and flame.
    • Keep out of reach of children
    • In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately

    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

    Other Information:

    • Do not  store above 105℃
    • May discolor some fabrics
    • Harmful to wood finishes and plastics
  • Directions

    • Wet hands thoroughly with product and rub unitl dry without wiping.
    • For children under 6, use only under adult supervision.
    • Not recommended for infants.
  • Inactive ingredients

    Water, Glycerin, Carbomer, Propylene Glycol, Sodium Hydroxide, Fragrance

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    PEANNUTS HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74274-120
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL68 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74274-120-0129 mL in 1 BOTTLE; Type 0: Not a Combination Product12/03/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/03/2020
    Labeler - Huizhou Bliss Commodity Co., Ltd (417467331)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huizhou Bliss Commodity Co., Ltd417467331manufacture(74274-120)
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