Label: LOCKE TEDDY FOAMING HAND SANITIZER- benzalkonium chloride solution

  • NDC Code(s): 73928-011-01, 73928-011-02, 73928-011-03, 73928-011-04, view more
    73928-011-05, 73928-011-06, 73928-011-07, 73928-011-08, 73928-011-09, 73928-011-10
  • Packager: KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD
  • 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 March 30, 2021

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

  • Drug facts

  • Active ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Antimicrobial 

  • Uses

    1. for hand sanitizing to decrease the bacteria on the skin
    2. recommended for repeated use

  • Warnings

    For external use only. 

    When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

    Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

  • Keep out of reach of children

     if swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    1. pump a small amount of foam into palm of hand 
    2. rub thoroughly over all surfaces of both hands 
    3. rub hands together briskly until dry 
  • Inactive ingredients

    Water, cetrimonium chloride, Laurtrimonium chloride, Dihydroxyethyl Cocamine oxide, citric acid, glycereth-17 cocoate

  • Product label

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  • INGREDIENTS AND APPEARANCE
    LOCKE TEDDY FOAMING HAND SANITIZER 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73928-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73928-011-0130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2021
    2NDC:73928-011-0250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2021
    3NDC:73928-011-0360 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2021
    4NDC:73928-011-04200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2021
    5NDC:73928-011-05250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2021
    6NDC:73928-011-06300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2021
    7NDC:73928-011-07400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2021
    8NDC:73928-011-08500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2021
    9NDC:73928-011-091000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2021
    10NDC:73928-011-102000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/23/2021
    Labeler - KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD (545349263)
    Establishment
    NameAddressID/FEIBusiness Operations
    KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD545349263manufacture(73928-011)