Label: PHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - SWEET PEA- alcohol gel

  • NDC Code(s): 76176-074-01
  • Packager: Ningbo Liyuan Daily Chemical Products 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 June 1, 2018

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  • Active Ingredient

    Ethyl Alcohol 62.0%

  • Purpose

    Antimicrobial

  • Uses

    - Helps reduce bacteria on the skin that could cause disease.

    Recommended for repeated use.

  • Warnings

    For external use only.

    Flammable. Keep away from fire or flame.

  • When using this product

    do not use in or near the eyes. In case of eye contact, flush eyes thoroughly with water.

  • Stop use and ask a doctor if:

    irritation and redness develops and lasts more than 72 hours.

  • Keep out of reach of children.

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

  • Directions-

    Place enough product in palm to thoroughly cover your hands. Rub hands together briskly until dry.

    Children under 6 years of age should be supervised when using this product.

  • OTHER SAFETY INFORMATION

    Other information: Store below 110 Fahrenheit degree (43 degrees Celsius)

    May discolor certain fabrics or surfaces.

  • Inactive Ingredients:

    Water, Aloe Barbadensis Gel, Carbomer, Fragrance, Glycerin, Triethanolamine, Tocopheryl Acetate, (Sweet Pea FD&C Red No. 33, FD&C Blue No.1)

  • Drug Facts

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    PHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - SWEET PEA 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76176-074
    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
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76176-074-0153 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/01/2018
    Labeler - Ningbo Liyuan Daily Chemical Products Co.,Ltd. (530766098)
    Registrant - Ningbo Liyuan Daily Chemical Products Co.,Ltd. (530766098)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Liyuan Daily Chemical Products Co.,Ltd.530766098manufacture(76176-074)
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