Label: 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 November 4, 2020

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

View All Sections
  • ACTIVE INGREDIENT

    Active ingredients

    Ethyl Alcohol 70%（V/V）

  • PURPOSE

    Antiseptic

  • WARNINGS

    Warnings:

    Flammable. Keep away from fire or flame. For external use only. Keep out of reach of children. Keep out of reach of eyes.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • ASK DOCTOR

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • INDICATIONS & USAGE

    Uses：

    For hand sanitizing to reduce bacteria on the skin.

  • DOSAGE & ADMINISTRATION

    Directions:

    Squeeze small amount in your palm and briskly rub hands together until dry.

  • OTHER SAFETY INFORMATION

    Other information

    Store between 15-30℃（59-86℉）
    Avoid freezing and excessive heat above 40℃（104℉）

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Water,Glycerin,Aloe Barbadensis Leaf Juice,Carbomer,Triethanolamine,Fragrance

  • PRINCIPAL DISPLAY PANEL

    100ml

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47993-242
    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
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47993-242-01100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/27/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/27/2020
    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!