Label: ANTIBACTERIAL WET WIPES- benzalkonium chloride cloth

  • NDC Code(s): 70412-500-10, 70412-500-50
  • Packager: Zhejiang Ayan Biotech Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

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

View All Sections
  • Drug Facts

  • Active Ingredient

    Benzalkonium Chloride (0.13%)

    Purpose

    Antiseptic

  • Uses

    For hand-washing to decrease bacteria on skin

  • Warnings

    Flammable. Keep away from heat and flame.

    For External use only.

    Do not use

    in eyes. In case of contact, rinse thoroughly with water.

    Stop use & ask doctor

    if rash/redness or irritation appears/develops and persist for more than 72 hours.

    Keep out of reach from children

    except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

  • Directions

    • Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation.
    • Thoroughly wipe hands, allow to dry without rinsing.
    • Discard after single use
  • Other information

    • Do not flush down toilet.
    • Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit)
    • May discolor certain fabrics
  • Inactive Ingredients

    Water(aqua), Propylene Glycol, Tocopherol, Kathon

  • Package Labeling:

    Label4

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL WET WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70412-500
    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)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    OCTHILINONE (UNII: 4LFS24GD0V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70412-500-1010 in 1 BOX04/15/2020
    15 g in 1 PATCH; Type 0: Not a Combination Product
    2NDC:70412-500-5050 in 1 BOX07/15/2020
    23.6 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/15/2020
    Labeler - Zhejiang Ayan Biotech Co.,Ltd. (544377996)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Ayan Biotech Co.,Ltd.544377996manufacture(70412-500)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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