Label: PHARMACYS PRESCRIPTION HAND SANITIZER 2OZ- ethyl alcohol gel

  • NDC Code(s): 76176-114-01, 76176-114-02
  • 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 October 1, 2018

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  • Drug Facts Active ingredients

    Ethyl Alcohol 62 percent

  • Purpose

    Antiseptic

  • Uses

    Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

  • Warnings

    For external use only.

    Do not swallow.

    Flammable. Keep away from fire or flame.

    Do not apply around eyes. Do not use in ears & mouth.

    When using this product, Avoid contact with eyes. In case of contact, flush eyes with water.

  • Stop use and ask a doctor if

    redness or irritation develops and persists for more than 72 hours.

  • Keep out of reach of children.

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

  • Directions

    pump as needed into your palms and thoroughly spread on both hands, rub into skin until dry.

  • Other information

    store at 20 Degree Celsius (68 to 77 Fahrenheit).

    may discolor fabrics.

  • Inactive ingredients

    water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, aloe barbadensis gel, carbomber, fragrance.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    PHARMACYS PRESCRIPTION HAND SANITIZER 2OZ 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76176-114
    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)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER 934 (UNII: Z135WT9208)  
    TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76176-114-01118.28 mL in 1 BOX; Type 0: Not a Combination Product10/01/2018
    2NDC:76176-114-0259.14 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A10/01/2018
    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(76176-114)
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