Label: HAND SANITIZER- ethyl alcohol liquid

  • NDC Code(s): 47993-328-01
  • Packager: NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD
  • 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 17, 2021

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

View All Sections
  • ACTIVE INGREDIENT

    Active ingredients

    Ethanol Alcohol 71% v/v

  • 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, Glycerin, Propylene Glycol, Fragrance, Aloe Barbedensis Leaf Juice, Tocopherol Acetate (VITAMIN E)

  • OTHER SAFETY INFORMATION

    Other information:

    Store below 106℉(41℃).

    May discolor certain fabrics.

  • 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 Paper card 1image of Paper card 2image of hand sanitizer 29.87ml

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47993-328
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL71 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47993-328-0129.87 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/16/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/16/2021
    Labeler - NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD (529334491)
    Registrant - NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD (529334491)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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