Label: WET WIPE- benzalkonium chloride swab

  • NDC Code(s): 76906-002-01, 76906-002-02, 76906-002-04, 76906-002-05, view more
    76906-002-06, 76906-002-07, 76906-002-08, 76906-002-09, 76906-002-10, 76906-002-11, 76906-002-12
  • Packager: Yiwu Beitao Infant & Mother Supplies Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 15, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active Ingredient

    Benzalkonium Chloride 0.13%

    Purpose

    Antimicrobial

  • USE

    For hand washing to decrease bacteria on the skin.
    Recommended for repeated use.

  • Warning

    For external use only
    When using this product, avoid contact with the eyes.
    In case of contact, flush eyes thoroughly with water.
    Stop use and ask a doctor if irritation and redness develop.

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

  • Directions

    For hand sanitizing to decrease bacteria on the skin.
    Recommended for repeated use.

  • Inactive ingredients

    Aqua, Propylene Glycol, Polysorbate 20, Phenoxyethanol.

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    WET WIPE 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76906-002
    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
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76906-002-07100 in 1 BOX03/21/2020
    14.8 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:76906-002-08135 in 1 PAIL03/21/2020
    22.07 g in 1 POUCH; Type 0: Not a Combination Product
    3NDC:76906-002-0110 in 1 BAG03/21/2020
    35 g in 1 POUCH; Type 0: Not a Combination Product
    4NDC:76906-002-0450 in 1 BAG03/21/2020
    46 g in 1 POUCH; Type 0: Not a Combination Product
    5NDC:76906-002-0220 in 1 BAG03/21/2020
    56.5 g in 1 POUCH; Type 0: Not a Combination Product
    6NDC:76906-002-05350 in 1 BAG03/21/2020
    65.8 g in 1 POUCH; Type 0: Not a Combination Product
    7NDC:76906-002-0680 in 1 BAG03/21/2020
    75.25 g in 1 POUCH; Type 0: Not a Combination Product
    8NDC:76906-002-09250 in 1 PAIL03/21/2020
    82.08 g in 1 POUCH; Type 0: Not a Combination Product
    9NDC:76906-002-1060 in 1 PAIL03/21/2020
    95.83 g in 1 POUCH; Type 0: Not a Combination Product
    10NDC:76906-002-1125 in 1 BAG03/21/2020
    108 g in 1 POUCH; Type 0: Not a Combination Product
    11NDC:76906-002-12100 in 1 BAG03/21/2020
    114.8 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/21/2020
    Labeler - Yiwu Beitao Infant & Mother Supplies Co., Ltd. (412925352)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yiwu Beitao Infant & Mother Supplies Co., Ltd.412925352manufacture(76906-002)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!