Label: NONGBIAE HAND SANITIZER- ethyl alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated November 16, 2021

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

View All Sections
  • Active Ingredient

    Ethyl Alcohol 60%

  • Purpose

    Antiseptic

  • Uses

    Hand sanitizer to decrease bacteria on the skin that could cause disease.

  • Warnings

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

  • Do not use

    Stop using it if you have severe red spots or itching.

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Stop use

    Stop use and ask a doctor if irritation or rash occurs.

  • When using

    ·Keep out of eyes. In case of contact with eyes, flush thoroughly with water. ·Avoid contact with broken skin.

    ·Do not inhale or ingest.

  • Directions

    Place enough product on hands to cover all surfaces.

    Rub hands together until dry.

    Supervise children under 6 years of age when using this product to avoid swallowing.

  • Inactive Ingredients

    Water, Citric acid, Protein, Fatty acid ester, Glycerin

  • Label

    NONGBIAE Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    NONGBIAE HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82390-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROLYZED ORYZANOL (UNII: 3OE0DD1I5J)  
    ISOPROPYL BEHENATE (UNII: 1BWO0L9BHI)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82390-102-01100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/16/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/16/2021
    Labeler - Evergreenplus (695376425)
    Establishment
    NameAddressID/FEIBusiness Operations
    Evergreenplus695376425manufacture(82390-102)
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!