Label: REDDY LAB ADVANCED ALCOHOL GEL SANITIZER- alcohol gel

  • NDC Code(s): 79671-797-04
  • Packager: Flavor Reddy Foods, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 13, 2024

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

  • ACTIVE INGREDIENT

    Active Ingredient

    Ethyl Alcohol 70%

  • WARNINGS

    Wanings

    • For external use only. Do not ingest
    • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
    • FLAMMABLE. This product contains ethyl alcohol.
    • Keep away from sources of ignition.
    • Discontinue use if irritation or redness develops.
    • If irritation persists for more than 72 hours, contact a physician.
    • KEEP OUT OF THE REACH OF CHILDREN
    • IF swallowed, get medical help or contact a Poison Control Center right away.
  • INACTIVE INGREDIENT

    Water, Glycerin, PEG-6 (and) AMP - Acrylates/Vinyl Isodecanoate Crosspolymer, Diisopropanolamine, Aloe Barbadensis Leaf Juice.

  • PURPOSE

    Anitseptic

  • DOSAGE & ADMINISTRATION

    Directions

    • Read the entire label before using this product.
    • Place enough product on your palm to thoroughly cover your hands.
    • Rub hands together briskly until dry.
  • INDICATIONS & USAGE

    Uses

    • Hand sanitizer to reduce microorganisms on the skin
    • Use thi product when soap and water are not available
  • KEEP OUT OF REACH OF CHILDREN

    • KEEP OUT OF REACH OF CHILDREN
  • PRINCIPAL DISPLAY PANEL

    Display Panel Label

  • INGREDIENTS AND APPEARANCE
    REDDY LAB ADVANCED ALCOHOL GEL SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79671-797
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79671-797-043780 mL in 1 JUG; Type 0: Not a Combination Product01/28/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/28/2021
    Labeler - Flavor Reddy Foods, LLC (095736309)
    Registrant - Betco Corporation Ltd (005050158)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation Ltd005050158manufacture(79671-797) , label(79671-797)