Label: HAND SANITIZER gel

  • NDC Code(s): 72449-100-01, 72449-100-02, 72449-100-03, 72449-100-04, view more
    72449-100-05, 72449-100-06, 72449-100-07, 72449-100-08, 72449-100-09, 72449-100-10, 72449-100-11
  • Packager: LS Promotions Inc.
  • 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 December 9, 2020

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  • Drug Facts

    Drug Facts

  • Active Ingredients

    Ethyl Alcohol

  • Purpose

    Antiseptic

  • Uses

    • To help decrease bacteria on hands.
  • Warnings

    • For external use only
    • Flammable, keep away from fire or flame
  • When using this product

    • Keep out of eyes
    • In case of contact with eyes, flush thoroughly with water and then seek medical advise
  • Stop use and ask a doctor

    • If irritation or redness develops
  • Keep out of reach of children

    • If swallowed, get medical help or contact a poison control center immediately
  • Directions

    • Place enough product in your palm to thoroughly cover hand.
    • Rub hands together briskly until dry.
    • For children under 6 years old, use adult supervision.
  • Other information

    • Do not store above 100°F
  • Inactive Ingredients

    Inactive ingredients: water, glycerin, propylene glycol, carbomer, triethanolamine, isopropyl myristate, aloe vera oil, fragrance

  • Questions or Comments?

    Call weekdays from 9 AM to 5 PM EST at 631-231-2300 - www.lancopromo.com

  • Principal display panel

    ABL1900 Hand Sanitizer GelABL1900 Hand Sanitizer Gel NDC # 72449-100-03

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72449-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER 1342 (UNII: 809Y72KV36)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA WHOLE (UNII: KIZ4X2EHYX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72449-100-03236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2020
    2NDC:72449-100-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2020
    3NDC:72449-100-05473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2020
    4NDC:72449-100-0659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2020
    5NDC:72449-100-012.9 mL in 1 PACKET; Type 0: Not a Combination Product03/23/2020
    6NDC:72449-100-025.9 mL in 1 PACKET; Type 0: Not a Combination Product03/23/2020
    7NDC:72449-100-0729 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2020
    8NDC:72449-100-08295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2020
    9NDC:72449-100-09354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/23/2020
    10NDC:72449-100-103785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2020
    11NDC:72449-100-11946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/23/2020
    Labeler - LS Promotions Inc. (024818391)
    Registrant - LS Promotions Inc. (024818391)
    Establishment
    NameAddressID/FEIBusiness Operations
    LS Promotions Inc.024818391manufacture(72449-100)
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