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PDI Sani-Hands Instant Hand Sanitizing Wipes (Profesional Disposables International, Inc.)

Available Formats

Dosage Form Package Information Links
CLOTH 83 mL in 1 PACKAGE (10819-5808-1) Label Information

Complete PDI Sani-Hands Instant Hand Sanitizing Wipes Information

  • Uses

    • Antiseptic
    • For hand washing to decrease bacteria on the skin.
    • Recommended 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 persist for more than 72 hours consult a physician.
    • If swallowed, get medical help or contact a Poison Control Center immediately.


    Keep out of reach of children

    unless under adult supervision.


  • Directions


    • Peel back label slowly
    • Pull out wipe and reseal label
    • Unfold and use
    • Wipe hands, fingers, interdigital areas and wrists thoroughly with towelettes. Be sure to utilize the entire wipe surface. Allow to dry.
    • If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe. Sanitize with a second wipe.
    • Discard after single use.

  • Other information

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

    Dosage

    Use first wipe to clean hands, then discard wipe. Sanitize with a second wipe.


  • Inactive ingredients

    Water, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate


  • Manufactured for:

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

    www.pdipdi.com


  • Active ingredient

    Alcohol 65.9% by volume


  • Purpose

    Antiseptic


  • Principal Display Panel - 20 Count

    lid: label

    flowrap: flowrap


  • INGREDIENTS AND APPEARANCE
    PDI SANI-HANDS INSTANT HAND SANITIZING WIPES 
    alcohol cloth
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:10819-5808
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.659 mL  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10819-5808-1 83 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/01/2011
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 08/25/2011
    Labeler - Professional Disposables International, Inc. (800777117)
    Registrant - Professonal Disposables International, Inc (800777117)
    Establishment
    Name Address ID/FEI Business Operations
    Guy & O'Neill, Inc. 926830563 manufacture(10819-5808)