Label: ANTIBACTERIAL WET WIPES- benzalkonium chloride swab

  • Contains inactivated NDC Code(s)
    NDC Code(s):
    69821-001-01, 69821-001-02, 69821-001-03, 69821-001-04, view more
    69821-001-05, 69821-001-06, 69821-001-07, 69821-001-08, 69821-001-09, 69821-001-10, 69821-001-11, 69821-001-12, 69821-001-13, 69821-001-14, 69821-001-15, 69821-001-16, 69821-001-17, 69821-001-18, 69821-001-19, 69821-001-20, 69821-001-21, 69821-001-22, 69821-001-23, 69821-001-24, 69821-001-25, 69821-001-26, 69821-001-27
  • Packager: Zhejiang Qimei Commodity 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 November 2, 2022

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

  • Active ingredient

    benzalkonium chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    for hand washing to decrease bacteria on skin

  • Warnings

    For External use only.
    Do not use if you are allergic to any of the ingredients.
    When using this product Do not get into eyes,if contact occurs ,rinse throughly with water.
    Discontinue use if irritation or redness develops if condition persists for more than 72 hours consults a physician.

  • Keep out of reach of children

    keep out of reach of children unless under adult supervision .if seallowed ,get medical help or contact a Poison Control Center immediately.

  • Directions

    Thoroughly wipe hands or face with wipe,Discard in trash receptacle;do not flush.Be sure to reseal label complete to retain moisture

  • INACTIVE INGREDIENT

    WATER PROPYLENE GLYCOL OCTHILINONE .ALPHA.-TOCOPHEROL

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL WET WIPES 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69821-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69821-001-0110 in 1 PACKAGE06/01/2017
    10.0042 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:69821-001-0215 in 1 PACKAGE06/01/2017
    20.0042 g in 1 POUCH; Type 0: Not a Combination Product
    3NDC:69821-001-0330 in 1 PACKAGE06/01/2017
    30.0042 g in 1 POUCH; Type 0: Not a Combination Product
    4NDC:69821-001-0450 in 1 PACKAGE06/01/2017
    40.0042 g in 1 POUCH; Type 0: Not a Combination Product
    5NDC:69821-001-0580 in 1 PACKAGE06/01/2017
    50.0042 g in 1 POUCH; Type 0: Not a Combination Product
    6NDC:69821-001-06100 in 1 PACKAGE06/01/2017
    60.0042 g in 1 POUCH; Type 0: Not a Combination Product
    7NDC:69821-001-0730 in 1 BOTTLE06/01/2017
    70.0042 g in 1 POUCH; Type 0: Not a Combination Product
    8NDC:69821-001-0850 in 1 BOTTLE06/01/2017
    80.0042 g in 1 POUCH; Type 0: Not a Combination Product
    9NDC:69821-001-0980 in 1 BOTTLE06/01/2017
    90.0042 g in 1 POUCH; Type 0: Not a Combination Product
    10NDC:69821-001-10100 in 1 BOTTLE06/01/2017
    100.0042 g in 1 POUCH; Type 0: Not a Combination Product
    11NDC:69821-001-111 in 1 BAG06/01/2017
    110.0042 g in 1 POUCH; Type 0: Not a Combination Product
    12NDC:69821-001-12250 in 1 CANISTER06/01/2017
    120.0042 g in 1 POUCH; Type 0: Not a Combination Product
    13NDC:69821-001-13800 in 1 BAG06/01/2017
    130.0042 g in 1 POUCH; Type 0: Not a Combination Product
    14NDC:69821-001-141000 in 1 BAG06/01/2017
    140.0042 g in 1 POUCH; Type 0: Not a Combination Product
    15NDC:69821-001-151200 in 1 BAG06/01/2017
    150.0042 g in 1 POUCH; Type 0: Not a Combination Product
    16NDC:69821-001-161500 in 1 BAG06/01/2017
    160.0042 g in 1 POUCH; Type 0: Not a Combination Product
    17NDC:69821-001-1716 in 1 BAG06/01/2017
    170.0042 g in 1 POUCH; Type 0: Not a Combination Product
    18NDC:69821-001-188 in 1 BAG06/01/2017
    180.36 g in 1 POUCH; Type 0: Not a Combination Product
    19NDC:69821-001-195 in 1 BAG06/01/2017
    19225 g in 1 POUCH; Type 0: Not a Combination Product
    20NDC:69821-001-2020 in 1 BAG06/01/2017
    200.9 g in 1 POUCH; Type 0: Not a Combination Product
    21NDC:69821-001-212000 in 1 BAG06/01/2017
    215.096 g in 1 POUCH; Type 0: Not a Combination Product
    22NDC:69821-001-221600 in 1 BAG06/01/2017
    224.077 g in 1 POUCH; Type 0: Not a Combination Product
    23NDC:69821-001-231800 in 1 BAG06/01/2017
    234.587 g in 1 POUCH; Type 0: Not a Combination Product
    24NDC:69821-001-242500 in 1 BAG06/01/2017
    246.37 g in 1 POUCH; Type 0: Not a Combination Product
    25NDC:69821-001-2560 in 1 BAG06/01/2017
    256.37 g in 1 POUCH; Type 0: Not a Combination Product
    26NDC:69821-001-26120 in 1 BAG06/01/2017
    266.37 g in 1 POUCH; Type 0: Not a Combination Product
    27NDC:69821-001-27150 in 1 PAIL06/01/2017
    276.37 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/06/2015
    Labeler - Zhejiang Qimei Commodity Co.,Ltd. (544331136)
    Registrant - Zhejiang Qimei Commodity Co.,Ltd. (544331136)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Qimei Commodity Co.,Ltd.544331136manufacture(69821-001)