Label: ALLPURE HAND SANITIZER- alcohol gel

  • NDC Code(s): 80176-002-01, 80176-002-02, 80176-002-03, 80176-002-04, view more
    80176-002-05, 80176-002-06, 80176-002-07
  • Packager: CERCI KOZMETIK VE OTEL EKIPMANLARI PAZARLAMA IC VE DIS TICARET LIMITED SIRKETI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 26, 2023

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

View All Sections
  • Active Ingredient

    Ethyl Alcohol 70% v/v.

  • Purpose

    Antiseptic

  • Use

    Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

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

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product keepout of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

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

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • 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.
  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)
  • Inactive ingredients

    Ipa, Carbomer, Glycerin, Purified Water, Rosmarinus Officinalis Extract, Triethanolamine

  • Package Label - Principal Display Panel

    Label

  • INGREDIENTS AND APPEARANCE
    ALLPURE HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80176-002
    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
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ROSEMARY (UNII: IJ67X351P9)  
    METHYL BENZOATE (UNII: 6618K1VJ9T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80176-002-0130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/20/2020
    2NDC:80176-002-0250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/20/2020
    3NDC:80176-002-03100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/20/2020
    4NDC:80176-002-04250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/20/2020
    5NDC:80176-002-05500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/20/2020
    6NDC:80176-002-061000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/20/2020
    7NDC:80176-002-075000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/20/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/20/2020
    Labeler - CERCI KOZMETIK VE OTEL EKIPMANLARI PAZARLAMA IC VE DIS TICARET LIMITED SIRKETI (502990784)
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!