NUVALU INSTANT HAND SANITIZER ORIGINAL (ETHYL ALCOHOL) GEL [NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.]

NUVALU INSTANT HAND SANITIZER ORIGINAL (ETHYL ALCOHOL) GEL [NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.]
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NDC 76176-212-01, 76176-212-36
Set ID 7b4fc1c0-4ea6-f047-e053-2a91aa0a1246
Category HUMAN OTC DRUG LABEL
Packager Ningbo Liyuan Daily Chemical Products Co., Ltd.
Generic Name
Product Class
Product Number
Application Number PART333A
  • INSTANT HAND SANITIZER

    helps fight germs without needing to wash your hands

    Take it with you when you are on the go

    Fight germs, anywhere, anytime.

    Use anyplace:

    Home

    School

    Work

    Outdoors

    Carry in:

    Purse

    Pocket

    Briefcase

    Backpack

    Glove box

  • Drug Facts Active Ingredient

    Ethyl Alcohol 70 percent

  • Purpose

    Antimicrobial

  • Uses

    Helps reduce bacteria on the skin.

  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only.

  • When using the product

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

  • Stop use and ask doctor if

    irritation or rash appears and lasts.

  • Keep out of reach of children.

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

  • Directions

    • Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry.
    • Children under 6 years of age should be supervised when using this product.
  • Other Information

    • Store below 106 Fahrenheit (41 Degree Celsius)
    • May discolor certain fabrics or surfaces.
  • Inactive Ingredients:

    water (aqua), carbomer, fragrance, glycerin, propylene glycol, triethanolamine, tocophereyl acetate (vitamin E), aloe barbadensis leaf juice

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    NUVALU INSTANT HAND SANITIZER ORIGINAL 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76176-212
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER 934 (UNII: Z135WT9208)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CUPRIC BIS(TRIETHANOLAMINE) (UNII: YBM44X0B6H)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76176-212-36120 mL in 1 BLISTER PACK; Type 0: Not a Combination Product11/01/2018
    2NDC:76176-212-0159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/01/2018
    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(76176-212)

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