Label: RELIEF CHEMISTRY HAND SANITIZER- ethyl alcohol 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 January 6, 2021

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  • Active ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antimicrobial

  • Uses

    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. Highly flammable liquid and vapor. Causes serious eye irritation. Keep away from heat or flame.

  • Do Not Use

    • In children less than 2 months of age
    • On open skin wounds
  • When using this product

    When using this product avoid contact with eyes, ears, and mouth.

    In case of contact with eyes, rinse eyes thoroughly with water.

  • Stop use or ask a doctor if

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

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • Place enough amount 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 15-30 0C (59-86 0F)
    • Avoid freezing and excessive heat above 40 0C (104 0F)
  • Inactive ingredients

    hydroxypropyl guar, water, citric acid.

  • Relief Chemistry Hand Sanitizer jaguar 1 gal

    relief.jpg

  • INGREDIENTS AND APPEARANCE
    RELIEF CHEMISTRY HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73787-121
    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
    WATER (UNII: 059QF0KO0R)  
    GUARAPROLOSE (1300 MPA.S AT 1%) (UNII: 1530WMS90S)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73787-121-013785 mL in 1 BOTTLE; Type 0: Not a Combination Product06/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/11/2020
    Labeler - FGD, LLC (111927555)
    Establishment
    NameAddressID/FEIBusiness Operations
    Goodwin Co.806987483manufacture(73787-121)
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