SANI PROFESSIONAL BRAND SANI-HANDS BASICS BZKHAND WIPES HAND WIPES HAND WIPES HAND WIPES HAND WIPES HAND WIPES (BENZALKONIUM CHLORIDE) CLOTH [PROFESSIONAL DISPOSABLES INTERNATIONAL, INC.]

SANI PROFESSIONAL BRAND SANI-HANDS BASICS BZKHAND WIPES HAND WIPES HAND WIPES HAND WIPES HAND WIPES HAND WIPES (BENZALKONIUM CHLORIDE) CLOTH [PROFESSIONAL DISPOSABLES INTERNATIONAL, INC.]
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NDC 10819-7008-1
Set ID 7df54ea5-c4f5-4f63-8e34-72659f9265a3
Category HUMAN OTC DRUG LABEL
Packager Professional Disposables International, Inc.
Generic Name
Product Class
Product Number
Application Number PART333A
  • Use

    For hand washing to decrease bacteria on the skin

  • Warnings

    • For external use only.
    • If swallowed, get medical help or contact a Poison Control Center right away.
    • Do not use in the eyes.
    • Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a physician.
  • Inactive ingredients

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

  • Active ingredient

    Benzalkonium Chloride 0.13% w/w

  • Purpose

    Antiseptic handwash

  • Keep out of reach of children

    Keep out of reach of children unless under adult supervision.

  • Directions

    - To dispense, lift cover, remove seal, pull center sheet from roll, twist to a point, and feed through dispenser hole in cover. Keep cap closed to prevent moisture loss.

    - Use entire wipe to thoroughly wipe hands, fingers and wrists.

    - To sanitize, use multiple wipes.

    - Discard after single use.

  • Other Information

    Lot No. and Expiration Date can be found on canister.

  • Principal Display Panel - 150 Count Canister

    Front Canister Label

    front

    Back Canister Label
    back

  • INGREDIENTS AND APPEARANCE
    SANI PROFESSIONAL BRAND SANI-HANDS BASICS BZKHAND WIPES HAND WIPES HAND WIPES HAND WIPES HAND WIPES  HAND WIPES
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10819-7008
    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
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    SORBIC ACID (UNII: X045WJ989B)  
    PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MICROCITRUS AUSTRALIS FRUIT (UNII: 9DNS80T428)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10819-7008-16 in 1 CASE11/05/2013
    1933 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/201312/31/2022
    Labeler - Professional Disposables International, Inc. (800777117)
    Establishment
    NameAddressID/FEIBusiness Operations
    Professional Disposables International, Inc.800777117manufacture(10819-7008)

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