Label: NUVALU INSTANT HAND SANITIZER ALOE VERA- ethyl alcohol gel

  • NDC Code(s): 76176-211-01, 76176-211-36
  • 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 November 1, 2018

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  • 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 hear 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 the 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, FD&C Yellow No.5, FD&C Blue No.1

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    NUVALU INSTANT HAND SANITIZER ALOE VERA 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76176-211
    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)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    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:76176-211-36120 mL in 1 BLISTER PACK; Type 0: Not a Combination Product11/01/2018
    2NDC:76176-211-0159 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(76176-211)
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