Label: 8OZ INSTANT HAND SANITIZER LAVENDER- hand sanitizer liquid

  • NDC Code(s): 76176-563-01
  • Packager: Ningbo Liyuan Daily Chemical Products Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

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 February 1, 2017

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  • Drug Facts Active Ingredient

    Ethyl Alcohol 70% v/v

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  • Purpose

    Antimicrobial

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  • WARNINGS

    Flammable. Keep away from fire or flame.

    For external use only.

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  • When using this product,

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

    Stop use and ask doctor if irritation or rash appears and lasts.

    Keep out of reach for children. If swallowed, get medical help or contact a Posion Control Center right away.

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  • Keep out of reach of children.
  • Directions:

    . Place enough Product in your palm to thoroughtly spread on both hands and rub into the skin until dry.

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

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  • Other Information:

    . Store below 106℉. (41℃)

    . May discolor certail fabrics or surfaces

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  • INACTIVE INGREDIENTS:

    Water (Aqua), Lavandula Angustufolia (Lavender) Flower Extract, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, FD&C Blue No.1, FD&C Red No 33.

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  • INGREDIENTS AND APPEARANCE
    8OZ INSTANT HAND SANITIZER LAVENDER 
    hand sanitizer liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:76176-563
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R) 28 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:76176-563-01 1 in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/01/2017
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 02/01/2017
    Labeler - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)
    Registrant - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)
    Establishment
    Name Address ID/FEI Business Operations
    530766098 530766098 manufacture(76176-563)
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