Label: HUSKY 515 INSTANT HAND SANITIZER- ethanol gel

  • Category: HUMAN OTC DRUG LABEL

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 August 25, 2011

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient:

    Ethanol (60% v/v)

  • Purpose:

    Anti-Microbial Hand Sanitizer

  • Uses

    • Helps reduce bacteria that potentially can cause disease
    • Helps prevent cross contamination by hand contact
    • Recommended for repeated use
  • Warnings

    • For external use only
    • Flammable, keep away from fire, heat, or flame

    • Keep out of reach of children.

    Do not use near eyes

    • In case of eye contact flush with water for 15 minutes
    • If irritation persists stop use of product and get medical attention
    • In case of accidental ingestion seek medical attention or contact a poison control center immediately.
  • Directions

    • Use no water or towels
    • Apply appropriate amount of product to palm of hand
    • Rub until hands are completely covered
    • Agitate lightly until dry
    • Let air dry for 15 seconds
    • Do not rinse or wipe with towel.
  • Other Information

    • Store in a cool dry place below 104° F.
  • Inactive Ingredients

    Water, Carbomer, Triethanolamine, PEG-75 Lanolin, Aloe Vera Gel, Fragrance.

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel

    Bottle Label

    HUSKY®

    515

    INSTANT HAND

    SANITIZER

    (GEL-TYPE)

    • Enhanced with Moisturizers
    • Kills disease causing germs within seconds
    • Effective against MRSA, VRE, E. coli (0157:H7) Staphylococcus, Streptococcus and other organisms
    • Assists with OSHA Bloodborne Pathogen Standard Compliance

    For Hospital and Professional Use Only

    See Drug Facts panel for additional information.

    Bottle Label
  • INGREDIENTS AND APPEARANCE
    HUSKY 515   INSTANT HAND SANITIZER
    ethanol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63779-515
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    alcohol (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M) alcohol600 mL  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    carbomer homopolymer type c (UNII: 4Q93RCW27E)  
    aloe (UNII: V5VD430YW9)  
    trolamine (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63779-515-053.785 L in 1 BOTTLE
    2NDC:63779-515-150.044 L in 1 BOTTLE
    3NDC:63779-515-270.118 L in 1 BOTTLE
    4NDC:63779-515-620.237 L in 1 BOTTLE
    5NDC:63779-515-800.800 L in 1 BAG
    6NDC:63779-515-880.237 L in 1 BOTTLE
    7NDC:63779-515-890.490 L in 1 BOTTLE
    8NDC:63779-515-201.100 L in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/28/1998
    Labeler - Canberra Corporation (068080621)
    Establishment
    NameAddressID/FEIBusiness Operations
    Canberra Corporation068080621MANUFACTURE
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