Label: ASSORTED SCENTED HAND SANITIZERS- alcohol spray

  • NDC Code(s): 74274-016-01
  • Packager: Huizhou Bliss Commodity 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 May 22, 2020

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

View All Sections
  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 75%

  • Purpose

     Antiseptic

  • Use

    • To decrease bacteria on skin without soap or water
    • Recommended for repeated use
  • KEEP OUT OF REACH OF CHILDREN

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

  • warnings:

    Flamable, keep away from fire and flame.

    For external use only hands.

    Do not use in or near eye. In case of contact with, rinse thoroughly with water. 

    Stop use and ask a doctor

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

  • Directions

    • Put enough product on palm and rub hands until dry
    • Children under 6 year of age should be supervised while using this product
  • Inactive ingredients

    Aqua, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Glycerin, Tetrahydroypropyl Ethylenediamine, Peg-40 Hydrogenated Cator Oil, Perfume

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    ASSORTED SCENTED HAND SANITIZERS 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74274-016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    EDETOL (UNII: Q4R969U9FR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74274-016-016 in 1 BOTTLE, SPRAY05/22/2020
    17 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/22/2020
    Labeler - Huizhou Bliss Commodity Co., Ltd (417467331)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huizhou Bliss Commodity Co., Ltd417467331manufacture(74274-016)
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!