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

SANI PROFESSIONAL BRAND SANI-HANDS BASICSHAND WIPES HAND WIPES (BENZALKONIUM CHLORIDE) CLOTH [PROFESSIONAL DISPOSABLES INTERNATIONAL, INC.]
PDF | XML

NDC 10819-7007-1
Set ID ddeb9ae3-b6be-4633-9ac4-408cef1c105b
Category HUMAN OTC DRUG LABEL
Packager Professional Disposables International, Inc.
Generic Name
Product Class
Product Number
Application Number PART333A
  • Use

    - Hand sanitizer to decrease bacteria on the skin

    - For repeated use

    - Dries in seconds

  • Warnings

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

    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

    Antimicrobial

  • 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.

  • Keep out of reach of children

    Keep this out of reach of children

  • Other information

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

  • Principal Display Panel

    Front Canister Label:

    front

    Back Canister Label:

    back

  • INGREDIENTS AND APPEARANCE
    SANI PROFESSIONAL BRAND SANI-HANDS BASICSHAND WIPES  HAND WIPES
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10819-7007
    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
    PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    SORBIC ACID (UNII: X045WJ989B)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MICROCITRUS AUSTRALIS FRUIT (UNII: 9DNS80T428)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10819-7007-16 in 1 CASE03/01/2013
    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(10819-7007)

Related Drugs