Label: PDI SANI HANDS- instant hand sanitizing wipes cloth

  • NDC Code(s): 10819-3918-1
  • Packager: Professional Disposables International Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 12, 2023

If you are a consumer or patient please visit this version.

  • Active ingredient

    Alcohol 70% by volume

  • Purpose

    Antiseptic

  • Uses

    • Antiseptic.
    • For handwashing 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 conditions persist for more than 72 hours, consult a physician.

  • Keep this out of reach of children

    unless under adult supervision.

    if swallowed, get medical help or contact a Poison Control Center immediately

  • Directions

    • Peel back label slowly.
    • Pull out wipe and reseal label.
    • Unfold and use.
    • Wipe hands, fingers, interdigital areas and wrists thoroughly with towelette. 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.
  • inactive ingredients

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

  • Principal Display panel

    Web:

    web

    Reseal:

    reseal

  • INGREDIENTS AND APPEARANCE
    PDI SANI HANDS 
    instant hand sanitizing wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10819-3918
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10819-3918-120 in 1 CELLO PACK04/01/2016
    14.15 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/01/2016
    Labeler - Professional Disposables International Inc (800777117)
    Registrant - Professional Disposables International Inc (800777117)