Label: ANTIMICROBIAL HAND SANITIZER- alcohol gel

  • NDC Code(s): 51811-400-20, 51811-400-21, 51811-400-25, 51811-400-31, view more
    51811-400-40, 51811-400-41, 51811-400-44, 51811-400-45, 51811-400-50, 51811-400-51, 51811-400-52
  • Packager: HPC Ventures, LLC
  • This is a repackaged label.
  • Source NDC Code(s): 61010-7111
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 27, 2024

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  • Drug Facts

    Active Ingredient

    Ethyl Alcohol 70%

    Purpose

    Antiseptic

  • Uses

    • For handwashing to decrease bacteria on skin
    • Recommended for repeated use
  • Warnings

    For external use only

    Flammable, keep away from fire or flame

  • DO NOT USE

    Do not use in the eyes, if this happens reinse thoroughly with water.

  • ASK DOCTOR

    Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

    If ingested get medical help or contact a Poison Control Center right away

  • Directions

    • wet hands thoroughly with product allow to dry without wiping
    • children under six should be supervised while using this product
  • INACTIVE INGREDIENT

    Inactive Ingredients aloe vera, carbomer, purified water, triethanolamine

  • SPL UNCLASSIFIED SECTION

    Antimicrobial Hand Sanitizer Gel - Unscented ** fl. oz. Lot# ****

    Pkgd by HPC Global, Hanover PA, 17331 Made in USA

  • NDC 51811-400-20

    LABEL NDC 51811-400-20

  • NDC 51811-400-21

    NDC 51811-400-21

  • NDC 51811-400-25

    NDC 51811-400-25

  • NDC 51811-400-31

    NDC 51811-400-31

  • NDC 51811-400-40 and 51811-400-41

    NDC 51811-400-40 and 51811-400-41

  • NDC 51811-400-44 and 51811-400-45

    NDC 51811-400-44 and 51811-400-45

  • NDC 51811-400-50

    NDC 51811-400-50

  • NDC 51811-400-51 and 41811-400-52

    NDC 51811-400-51 and 51811-400-52

  • INGREDIENTS AND APPEARANCE
    ANTIMICROBIAL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51811-400(NDC:61010-7111)
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mg  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51811-400-200.029 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2020
    2NDC:51811-400-210.029 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
    3NDC:51811-400-250.029 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
    4NDC:51811-400-310.059 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
    5NDC:51811-400-400.118 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
    6NDC:51811-400-410.118 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/13/2010
    7NDC:51811-400-440.236 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
    8NDC:51811-400-450.236 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/13/2010
    9NDC:51811-400-500.473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
    10NDC:51811-400-510.473 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2020
    11NDC:51811-400-520.473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00309/13/2010
    Labeler - HPC Ventures, LLC (097538103)
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