WET NAPS ANTIBACTERIAL HAND WIPES FRESH (ANTIBACTERIAL HAND WIPES) SWAB [PROFESSIONAL DISPOSABLES INTERNATIONAL INC.]

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WET NAPS ANTIBACTERIAL HAND WIPES FRESH (ANTIBACTERIAL HAND WIPES) SWAB [PROFESSIONAL DISPOSABLES INTERNATIONAL INC.]
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NDC 10819-7011-1, 10819-7011-2, 10819-7011-3, 10819-7011-4, 10819-7011-5
Set ID bcfa4133-5eb8-42d0-b592-ba03a0345875
Category HUMAN OTC DRUG LABEL
Packager Professional Disposables International Inc.
Generic Name
Product Class
Product Number
Application Number PART333A
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  • Active Ingredient

    Benzalkonium chloride 0.13% w/w

  • Purpose

    Antiseptic handwash

  • Use

    For hand washing to decrease bacteria on the skin.

  • Warnings

    For external use only.

    Do not use in the eyes.

    Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

  • Keep out of reach of children

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

  • Directions

    Directions for container:

    • To dispense, lift cover, remove seal, pull center sheet from roll, twist to a point, feed through dispenser hole in cover. Keep lid closed to prevent moisture loss.
    • Use as part of your hand cleaning routine.
    • Run product onto hands and allow to dry.
    • Discard after single use.

    Directions for packets or flowrap: see on container the directions to retreive the wipe.

  • Inactive ingredients

    Purified Water, SD Alcohol 40, Sorbic Acid, PPG-2 Hydroxyethyl Cocamide, Disodium EDTA, Aloe Barbadensis Leaf Juice, Fragrance

  • Principal Display panel

    Wet Naps

    Antibacterial Hand Wipes

    Moisturizes with Aloe

    Kills 99.99% of Germs

    Fresh Scent

    Front Canister: front

    Back Canister: back

    Packet: packet

    Box: box

    flowrap: flowrap

    Bonus 30ct box: box-fresh 30ct

    Bonus 54ct canister: front fresh 54ct

  • INGREDIENTS AND APPEARANCE
    WET NAPS ANTIBACTERIAL HAND WIPES  FRESH
    antibacterial hand wipes swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10819-7011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    SORBIC ACID (UNII: X045WJ989B)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10819-7011-1193.1 mL in 1 CANISTER; Type 0: Not a Combination Product01/01/2014
    2NDC:10819-7011-224 in 1 BOX03/01/2014
    24.4 mL in 1 PACKET; Type 0: Not a Combination Product
    3NDC:10819-7011-320 in 1 CELLO PACK01/01/2016
    32.6 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    4NDC:10819-7011-430 in 1 BOX08/01/2016
    44.4 mL in 1 PACKET; Type 0: Not a Combination Product
    5NDC:10819-7011-5266 mL in 1 CANISTER; Type 0: Not a Combination Product08/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/201412/31/2022
    Labeler - Professional Disposables International Inc. (800777117)
    Registrant - Professional Disposables International Inc. (800777117)
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