Label: CABEAU SANITIZER TO GO- alcohol gel

  • NDC Code(s): 74274-014-01
  • Packager: Huizhou Bliss Commodity 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 May 7, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70%

  • Purpose

     Antiseptic

  • Use

    • to reduce bacteria on the skin that could cause disease
    • use when soap and water are not available.
  • KEEP OUT OF REACH OF CHILDREN

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

  • warnings:

    Flamable, keep away from heat and flames

    For external use only: hands

    Do not use:

    • on children less than 2 months of age
    • on open skin wounds

    When using this product

    • keep out of eyes. In case of contac with eyes, flush thoroughly with water
    • avoid contact with broken skin
    • do not inhale or ingest

    Stop use and ask a doctor if

    • Irritation or redness develop
    • condition persists for more than 72 hours
  • Directions

    • Wet hands thoroughly with product and rub hands until dry
    • for children under 6, use only under adult supervision to avoid swallowing
    • not for infants

    Other information:

    • do not store above 105℉
    • may discolor some fabrics
  • Inactive ingredients

    Water, glycerin, propyene glycol, carbomer, sodium hydroxide, fragrance

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    CABEAU SANITIZER TO GO 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74274-014
    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
    WATER (UNII: 059QF0KO0R)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74274-014-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/07/2020
    Labeler - Huizhou Bliss Commodity Co., Ltd (417467331)
    Registrant - Huizhou Bliss Commodity Co., Ltd (417467331)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huizhou Bliss Commodity Co., Ltd417467331manufacture(74274-014)
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

More Info on this Drug

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