Label: HAND SANITIZER gel

  • NDC Code(s): 47993-293-01
  • Packager: NINGBO JIANGBEI OCEAN STAR TRADING 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 November 5, 2020

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  • ACTIVE INGREDIENT

    Active ingredients

    Ethanol Alcohol 62%

  • PURPOSE

    Antiseptic

  • INDICATIONS & USAGE

    Uses：

    Hand sanitizer to help reduce germs on the skin. 

  • WARNINGS

    Warnings:

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

  • WHEN USING

    When using this product, do not use in or near the eyes. In case of contact, rinse thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if, irritation or rash appears and lasts.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center Immediately.

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water,Triethanolamine,Glycerin,Propylene,Glycol,Aloe barbadensis,Vitamin E

  • OTHER SAFETY INFORMATION

    Other information

    Store below 106℉(41℃)

    May discolor certain fabrics or surface

  • DOSAGE & ADMINISTRATION

    Directions:

    Spray product into palms and rub together until dry.

    Adult supervision is recommended for children under age 6.

  • PRINCIPAL DISPLAY PANEL

    image of hand sanitizer 29.87mlimage of Paper card 1image of Paper card 2

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47993-293
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 112 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE (UNII: AUG1H506LY)  
    ETHYLENE GLYCOL (UNII: FC72KVT52F)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47993-293-0129.87 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/09/2020
    Labeler - NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD (529334491)
    Registrant - NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD (529334491)
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