Label: BLUE CEDAR HAND SANITIZER- hand sanitizer gel

  • 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 June 22, 2020

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

  • DOSAGE & ADMINISTRATION

    1.Store between 15-30°C (59-86°F)
    2.Avoid freezing and excessive heat above 40°C (104°F)

  • INACTIVE INGREDIENT

    Water, Carbomer, Glycereth-26, Triethanolamine, Fragrance(Parfum)

  • INDICATIONS & USAGE

    1.Place enough product .on hands to cover all surfaces.Rub hands together until dry.
    2.Superise children under 6 years of age when using this product to avoid swallowing.

  • ACTIVE INGREDIENT

    Ethyl Alcohol

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    Disinfection
    Sterilization
    No Rinseing

  • WARNINGS

    For external use only. Flammable. Keep away from heat or flame

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    BLUE CEDAR HAND SANITIZER 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55444-005
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL750 mL  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code BlueCedar
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55444-005-011000 mL in 1 BOTTLE; Type 0: Not a Combination Product05/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/28/2020
    Labeler - Anhui Kiwi Biotech Co., Ltd. (554444636)
    Establishment
    NameAddressID/FEIBusiness Operations
    Anhui Kiwi Biotech Co., Ltd.554444636manufacture(55444-005)