Label: ANMEIKANG DISINFECTANT WIPES- disinfectant wipes cloth

  • Contains inactivated NDC Code(s)
    NDC Code(s):
    81496-002-01, 81496-002-02, 81496-002-03, 81496-002-04, view more
    81496-002-05, 81496-002-06, 81496-002-07, 81496-002-08, 81496-002-09, 81496-002-10, 81496-002-11, 81496-002-12, 81496-002-13
  • Packager: Liaoning MeiXin Pharmaceutical Company
  • 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 26, 2021

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

  • Active Ingredient

    Benzalkonium chloride 0.13% w/w

  • Purpose

    Antiseptic

  • Uses

    Suitable for wiping hands, face, skin and other unbroken skin.

  • Warnings

    For external use only.

    When using this product avoid to contact eyes, mouth, wounds and other sensitive parts. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

    The product is insoluble in water, do not dispose the used wet wipes into flush toilets.

    The product is disposable, for single use, please do not reuse.

  • Directions

    Open the buckle cover, take out the wet wipes, wipe directly on the skin, and close the seal immediately after use to avoid drying of wet wipes.

  • Other Information

    · Store in a cool, dry place, and avoid contact with direct sunlight and heat source.

    · Pay attention to environmental protection, please put them into the trash can after use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Inactive Ingredients

    Water, 2-phenoxyethanol, Fragrance (parfum), Didecyl dimethyl ammonium chloride, Propylene Glycol

  • PRINCIPAL DISPLAY PANEL

    10 PCS in bag, NDC: 81496-002-01

    10 in bag label

  • PRINCIPAL DISPLAY PANEL

    20 PCS in bag, NDC: 81496-002-02

    20 in bag label

  • PRINCIPAL DISPLAY PANEL

    30 PCS in bag, NDC: 81496-002-03

    30 in bag label

  • PRINCIPAL DISPLAY PANEL

    40 PCS in bag, NDC: 81496-002-04

    40 in bag label

  • PRINCIPAL DISPLAY PANEL

    50 PCS in bag, NDC: 81496-002-05

    50 in bag label

  • PRINCIPAL DISPLAY PANEL

    60 PCS in bag, NDC: 81496-002-06

    60 in bag label

  • PRINCIPAL DISPLAY PANEL

    80 PCS in bag, NDC: 81496-002-07

    80 in bag label

  • PRINCIPAL DISPLAY PANEL

    20 PCS in box, NDC: 81496-002-08

    20 in box label

  • PRINCIPAL DISPLAY PANEL

    30 PCS in box, NDC: 81496-002-09

    30 in box label

  • PRINCIPAL DISPLAY PANEL

    50 PCS in box, NDC: 81496-002-10

    50 in box label

  • PRINCIPAL DISPLAY PANEL

    60 PCS in canister, NDC: 81496-002-11

    60 in canister label

  • PRINCIPAL DISPLAY PANEL

    100 PCS in canister, NDC: 81496-002-12

    100 in canister label

  • PRINCIPAL DISPLAY PANEL

    120 PCS in canister, NDC: 81496-002-13

    120 in canister label

  • INGREDIENTS AND APPEARANCE
    ANMEIKANG DISINFECTANT WIPES 
    disinfectant wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81496-002
    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
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    WATER (UNII: 059QF0KO0R)  
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81496-002-0110 in 1 BAG03/01/2021
    10.00764 g in 1 PATCH; Type 0: Not a Combination Product
    2NDC:81496-002-0220 in 1 BAG03/01/2021
    20.00764 g in 1 PATCH; Type 0: Not a Combination Product
    3NDC:81496-002-0330 in 1 BAG03/01/2021
    30.00764 g in 1 PATCH; Type 0: Not a Combination Product
    4NDC:81496-002-0440 in 1 BAG03/01/2021
    40.00764 g in 1 PATCH; Type 0: Not a Combination Product
    5NDC:81496-002-0550 in 1 BAG03/01/2021
    50.00764 g in 1 PATCH; Type 0: Not a Combination Product
    6NDC:81496-002-0660 in 1 BAG03/01/2021
    60.00764 g in 1 PATCH; Type 0: Not a Combination Product
    7NDC:81496-002-0780 in 1 BAG03/01/2021
    70.00764 g in 1 PATCH; Type 0: Not a Combination Product
    8NDC:81496-002-0820 in 1 BOX03/01/2021
    80.00764 g in 1 POUCH; Type 0: Not a Combination Product
    9NDC:81496-002-0930 in 1 BOX03/01/2021
    90.00764 g in 1 POUCH; Type 0: Not a Combination Product
    10NDC:81496-002-1050 in 1 BOX03/01/2021
    100.00764 g in 1 POUCH; Type 0: Not a Combination Product
    11NDC:81496-002-1160 in 1 CANISTER03/01/2021
    110.00764 g in 1 PATCH; Type 0: Not a Combination Product
    12NDC:81496-002-12100 in 1 CANISTER03/01/2021
    120.00764 g in 1 PATCH; Type 0: Not a Combination Product
    13NDC:81496-002-13120 in 1 CANISTER03/01/2021
    130.00764 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/01/2021
    Labeler - Liaoning MeiXin Pharmaceutical Company (712964681)
    Registrant - Liaoning MeiXin Pharmaceutical Company (712964681)
    Establishment
    NameAddressID/FEIBusiness Operations
    Liaoning MeiXin Pharmaceutical Company712964681manufacture(81496-002)