Label: 2PACK 2OZ HAND SANITIZER- CLASSIC- hand sanitizer liquid

  • NDC Code(s): 76176-562-01
  • 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 February 8, 2017

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts Active Ingredient

    Ethyl Alcohol 62.0%

  • Purpose

    Antimicrobial

  • Uses

    Hand Santizer to help reduce bacteria on skin.

  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only.

  • Keep out of reach of children.

  • 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.

  • 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.

  • Other Information:

    . Store below 106℉. (41℃)

    . May discolor certail fabrics or surfaces

  • Inactive Ingredients:

    Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine, FD&C Blue No.1, FD&C Yellow No 5.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    2PACK 2OZ HAND SANITIZER- CLASSIC 
    hand sanitizer liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76176-562
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 36 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76176-562-011 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/02/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/02/2017
    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(76176-562)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!