Label: INSTANT HAND SANITIZER- alcohol gel

  • NDC Code(s): 61010-1112-1, 61010-1112-2, 61010-1112-3, 61010-1112-8
  • Packager: Safetec of America
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 16, 2024

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

  • Active ingredient

    Ethyl Alcohol 66.5%

  • Purpose

    Antiseptic

  • Uses

    • For handwashing to decrease bacteria on skin without soap and water
  • Warnings

    For external use only

    Flammable, keep away from fire or flame.

    Keep out of reach of children.

    Do not usein eyes, if this happens, rinse thoroughly with water.

    Stop use, ask a doctor ifirritation develops and persists for 72 hours. If ingested, get medical help or contact a Poison Control Center right away.

  • Directions

    • wet hands & wrists thoroughly with product and allow to dry without wiping
  • Inactive ingredients

    aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

  • PRINCIPAL DISPLAY PANEL – 0.9g Pouch Label

    Safetec

    A.B.H.C. ™ MEETS CDC HANDWASHING RECOMMENDATIONS

    Instant
    Hand
    Sanitizer

    0.9 g (1/32 oz.)

    Safetec of America, Inc.

    Buffalo, NY 14215

    800-456-7077

    PRINCIPAL DISPLAY PANEL – 0.9g Pouch Label
  • PRINCIPAL DISPLAY PANEL – 144 Packets Box Label

    NDC 61010-1112-3

    Safetec

    Infection Control

    Instant Hand Sanitizer

    Fresh Scent Instant
    Hand Sanitizer with
    Aloe Vera

    A.B.H.C. ™ MEETS CDC HANDWASHING RECOMMENDATIONS

    144 Packets

    Each Packet Net. Wt. 0.9g

    PRINCIPAL DISPLAY PANEL – 144 Packets Box Label
  • INGREDIENTS AND APPEARANCE
    INSTANT HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61010-1112
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 665 mL  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    ALOE (UNII: V5VD430YW9)  
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61010-1112-225 in 1 BOX12/15/2010
    1NDC:61010-1112-10.034 L in 1 POUCH; Type 0: Not a Combination Product
    2NDC:61010-1112-3144 in 1 BOX12/15/2010
    2NDC:61010-1112-10.034 L in 1 POUCH; Type 0: Not a Combination Product
    3NDC:61010-1112-810 in 1 BOX04/01/2020
    3NDC:61010-1112-10.034 L in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/15/2010
    Labeler - Safetec of America (874965262)
    Establishment
    NameAddressID/FEIBusiness Operations
    Safetec of America, Inc.874965262manufacture(61010-1112)