Label: HYR HAND SANITIZER- ethanol liquid

  • 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 October 15, 2020

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Ethyl Alcohol 73%

  • PURPOSE

    Purpose

    Antimicrobial

  • INDICATIONS & USAGE

    Uses

    Hand sanitizing to help reduce bacteria on the skin

  • WARNINGS

    Warnings

    For external use only.

    Flammable. Keep away from fire or flame.

    When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

    ​Stop use and ask a doctor if irritation or redness appears and lasts

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

  • DOSAGE & ADMINISTRATION

    Directions

    Apply liberally to hands and gently rub until dry.

  • STORAGE AND HANDLING

    Other information

    Store above 0°C (32°F)

  • INACTIVE INGREDIENT

    Inactive ingredients

    purified water, isopropyl alcohol

  • SPL UNCLASSIFIED SECTION

    Distributed by: General Resources, LLC

    227 S. Smith Road, Suite 102, Tempe, AZ 85281

    www.gen-resources.com

  • PRINCIPAL DISPLAY PANEL

    HYR

    hand sanitizer

    ALCOHOL-BASED

    INSTANTLY KILLS 99.99% OF TESTED GERMS

    8 fl oz (236 mL)

    Proudly made in the USA

    70481-311 label 10-20

  • INGREDIENTS AND APPEARANCE
    HYR HAND SANITIZER 
    ethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70481-311
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL73 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70481-311-0660 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/05/2020
    2NDC:70481-311-24236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/05/2020
    3NDC:70481-311-263800 mL in 1 JUG; Type 0: Not a Combination Product04/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/05/2020
    Labeler - General Resources LLC (117648210)
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