Label: TRITON HS-777- alcohol soap

  • 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 November 12, 2012

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

  • Triton HS-777

    ​Active Ingredient

    Ethyl Alcohol 62%

  • Triton HS-777

    Uses

    • Hand sanitizer to reduce microorganisms on the skin.
    • Use in a variety of public settings when soap and water are not available.
  • Triton HS-777

    Warnings

    • For external use only.
    • FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition.
    • Children under the age of 6 should be supervised by an adult when using this product.
    • Discontinue use is irritation or redness develops.
    • KEEP OUT OF REACH OF CHILDREN.
  • Triton HS-777

    Directions

    • ​Read the entire label before using this product.
    • ​Apply a dime-sized amount (1.5 mL) of sanitizer on clean, dry hands.
    • Rub lightly into hands.
    • Let hands air dry.
  • Triton HS-777

    Inactive Ingredients

    ​Water, Glycerin, PPG-3 Benzyl Ether Myristate, Tetrahydroxypropyl Ethelendiamine, Carbomer, Fragrance, D&C Green #5.

  • Triton HS-777

    Questions or Comments?Phone: (800) 777-9343

    MDS information:​(800) 891-4965

  • Triton HS-777

    Purpose

    Antiseptic

  • Triton HS-777

    KEEP OUT OF REACH OF CHILDREN

  • Triton HS-777

    Triton HS-777

    INSTANT HAND SANITIZER

    Ethanol based Gel Hand Sanitizer

    Net Contents: 2L

    Item #77762-00

    MSDS No. 777

    2007 Betco Corporation

    Toledo, Ohio 43607-0127 Made in U.S.A.

    All Rights Reserved. www.betco.com

    77262.jpg

  • INGREDIENTS AND APPEARANCE
    TRITON HS-777 
    alcohol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65601-777
    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)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    EDETOL (UNII: Q4R969U9FR)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65601-777-622000 mL in 1 BOTTLE, DISPENSING
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E11/12/2012
    Labeler - Betco Corporation, Ltd. (005050158)
    Registrant - Betco corporation, Ltd. (005050158)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation, Ltd.005050158manufacture(65601-777)