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Sani Professional Brand Sanitizing Wipes (Professional Disposables International, Inc.)

Available Formats

Dosage Form Package Information Links
CLOTH 1250 BAG in 1 PAIL (10819-7002-2) > 4674 mL in 1 BAG Label Information

Complete Sani Professional Brand Sanitizing Wipes Information

  • 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 immediately.
    • Do not use in the eyes.
    • Flammable, keep away from fire or flame.
    • Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

    Keep out of reach of children.

  • Directions

    • 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.
    • Wet hands thoroughly with product and allow to dry without wiping.
    • Discard after single use.

  • Other information

    See bag label

    Dosage
    Wet hands thoroughly with product and allow to dry without wiping.

  • Inactive ingredients

    Water, SD Alcohol 40, Sorbic Acid, Cocamide DEA, Disodium EDTA, Aloe Barbadensis Leaf Juice, Fragrance


  • SPL UNCLASSIFIED SECTION

    Professional Disposables International, Inc.
    Orangeburg, NY 10962-1376 - USA - 1-800-999-6423
    Made in USA www.wipeyourworldclean.com


  • Principal Display Panel - 1250 Count

    Sani Professional Brand
    Sanitizing Wipes

    Kills 99.99% of Germs
    Cleans and Sanitizes with Every Wipe

    1250 Sanitizing Wipes [7.5 x 5.9 in (19.05 x 14.9 cm)]
    CAUTION: KEEP OUT OF REACH OF CHILDREN

    Bag Label

    Image of bag label

    Pail Label

    Image of pail label

  • Active ingredient

    Benzalkonium Chloride 0.13% w/w


  • Purpose

    Antiseptic handwash


  • INGREDIENTS AND APPEARANCE
    SANI PROFESSIONAL BRAND SANITIZING WIPES  
    benzalkonium chloride cloth
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:10819-7002
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride 0.13 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    SORBIC ACID (UNII: X045WJ989B)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MICROCITRUS AUSTRALIS FRUIT (UNII: 9DNS80T428)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10819-7002-2 1250 in 1 PAIL
    1 4674 mL in 1 BAG
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 01/01/2012
    Labeler - Professional Disposables International, Inc. (800777117)
    Establishment
    Name Address ID/FEI Business Operations
    Professional Disposables International, Inc. 800777117 manufacture(10819-7002)