Label: BLUE CEDAR HAND SANITIZER- hand sanitizer gel

  • 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 April 26, 2020

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

View All Sections
  • DOSAGE & ADMINISTRATION

    Store below 110°F (43° C).
    May discolor certain fabrics or surfaces.

  • WARNINGS

    Flammable. Keep away from fire or flame.

    Forexternal use only.

    Do not use this product in or near the eyes. In case of accidental contact, ninse eyes thoroughly with water.

    Stop use and ask doctor if iritation or rash appears andlasts.

    Keep away from children. If sallowed, get medicalhelp right away,

  • PURPOSE

    Kills Harmful Bacteria or Germs

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children.

  • INDICATIONS & USAGE

    Place enough product (1.5~-2 mL, about one full pump) in your palm to thoroughly cover your hands.

    Rub hands briskly until dry.

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

  • ACTIVE INGREDIENT

    Ethyl Alcohol 75土 59% 6(VW) or 65士5%

  • INACTIVE INGREDIENT

    Water, Carbomer, Glycereth :26, Triethanolamine, Fragrance (Parfum).

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    BLUE CEDAR HAND SANITIZER 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55444-002
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL44.25 mL  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    .ALPHA.-TERPINEOL (UNII: 21334LVV8W)  
    TERPINEOL (UNII: R53Q4ZWC99)  
    .GAMMA.-NONALACTONE (UNII: I1XGH66S8P)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorFRUITImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55444-002-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product03/21/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/21/2020
    Labeler - Anhui Kiwi Biotech Co., Ltd. (554444636)
    Establishment
    NameAddressID/FEIBusiness Operations
    Anhui Kiwi Biotech Co., Ltd.554444636manufacture(55444-002)
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!