Label: HAND SANITIZER gel

  • NDC Code(s): 67777-911-01, 67777-911-02, 67777-911-03, 67777-911-04, view more
    67777-911-05, 67777-911-06, 67777-911-07, 67777-911-08, 67777-911-09, 67777-911-10, 67777-911-11, 67777-911-12, 67777-911-13, 67777-911-14, 67777-911-15, 67777-911-16, 67777-911-17
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 3, 2025

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  • Active ingredient

    Alcohol 70% V/V

  • Purpose

    Antiseptic Handwash

  • Use

    For hand washing to decrease bacteria on the skin

  • Warnings

    For external use only

    Flammable: Keep away from fire or flame

    When using this product

    • Do not get in the eyes

    Stop use and ask a doctor if

    irritation and redness develop

    Keep out of reach of children.

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

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping

  • Other information

    • Store at room temperature (15º - 30ºC) (59º - 86ºF)

    • Recommended for repeated use

  • Inactive ingredients

    acrylates/C10-30 alkyl acrylate crosspolymer (60000 MPA.S), aloe barbadensis leaf juice, aminomethyl propanol, denatonium benzoate, fragrance, glycerin, propylene glycol, tocopheryl acetate, water

  • Label

    1427_BX_MASTER1427 Label

  • Label

    1428_BX_MASTER1428 Label

  • Label

    1429_BX_MASTER1429 Label

  • Label

    1431_IN_MASTER1431 Label

  • Label

    1432_IN_MASTER1432 Label

  • Label

    1433_BX_MASTER1433 Label

  • Label

    1433UB-10_BX_MASTER1433UB-10 Label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-911
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL 95% (UNII: 7528N5H79B) (ALCOHOL 95% - UNII:7528N5H79B) ALCOHOL 95%70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    AMINOMETHYL PROPANOL (UNII: LU49E6626Q)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Product Characteristics
    Color    Score    
    ShapeFREEFORMSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-911-036 in 1 CASE12/05/2025
    1NDC:67777-911-0224 in 1 BOX
    1NDC:67777-911-0129.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:67777-911-066 in 1 CASE12/05/2025
    2NDC:67777-911-0524 in 1 BOX
    2NDC:67777-911-0459 mL in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:67777-911-094 in 1 CASE12/05/2025
    3NDC:67777-911-0824 in 1 BOX
    3NDC:67777-911-07118.3 mL in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:67777-911-1148 in 1 CASE12/05/2025
    4NDC:67777-911-10236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:67777-911-1312 in 1 CASE12/05/2025
    5NDC:67777-911-12473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    6NDC:67777-911-1512 in 1 CASE12/05/2025
    6NDC:67777-911-14144 in 1 BOX
    61.01 mL in 1 PACKET; Type 0: Not a Combination Product
    7NDC:67777-911-17100 in 1 CASE12/05/2025
    7NDC:67777-911-1610 in 1 BOX
    71.01 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00312/05/2025
    Labeler - Dynarex Corporation (008124539)
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