Label: BLUE GUARD HAND SANITIZER- alcohol 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 May 22, 2020

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  • ACTIVE INGREDIENT

    Active ingredient                                  Purpose

    Ethyl Alcohol                70%      ...        Antimicrobial

  • PURPOSE

    Hand sanitizer to help decrease bacteria on the skin, when soap, water and towels are not available. Recommended for repeated use.

  • KEEP OUT OF REACH OF CHILDREN

    Ensure they are supervised when using this product.

  • INDICATIONS & USAGE

    keep out of eyes

    when water, soap and towel are not available

  • WARNINGS

    • For external use only.
    • Flammable. Keep away from fire or flame.
    • Do not use around eyes. In case of eyes contact, flush immediately with water
    • Do not use in ears or mouth
    • Stop use immediately and consult a physiccian if redness develops and persists for more than 72 hours.

    Other information:

    Store at 20℃ (68-70℉）

    May discolor fabrics

  • DOSAGE & ADMINISTRATION

    place enough product in your palm to thoroughly cover your hands. Rub hands together until dry

  • INACTIVE INGREDIENT

    Water, Aloe Barbadenis, Glycerin

  • PRINCIPAL DISPLAY PANEL

    image of label

  • INGREDIENTS AND APPEARANCE
    BLUE GUARD HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75780-004
    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)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER 934 (UNII: Z135WT9208)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75780-004-01150 mL in 1 BOTTLE; Type 0: Not a Combination Product05/22/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/22/2020
    Labeler - NINGBO MEINEKE Biotech Technology Co., Ltd. (413126185)
    Establishment
    NameAddressID/FEIBusiness Operations
    NINGBO MEINEKE Biotech Technology Co., Ltd.413126185manufacture(75780-004)
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