Label: ANTISEPTIC WIPES- zylast hand wipes swab

  • NDC Code(s): 57362-469-18, 57362-469-19
  • Packager: Westwood Laboratories
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2023

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  • ACTIVE INGREDIENT

    Ethyl Alcohol - 76%

  • PURPOSE

    Antiseptic

  • INDICATIONS & USAGE

    • To decrease bacteria on skin.
    • Recommended for repeated use.
  • WARNINGS

    • For external use only
    • Flammable. Keep away from flames or fires.
  • WHEN USING

    • Do not used in or near eyes.
    • In case of contact, wash eyes thoroughly with water.
    • Avoid contact with broken skin.
    • Do not inhale or ingest.
  • STOP USE

    • Irritiation or redness develops.
    • Condition persists for more than 72 hours.
  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or call a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    • Wet hands thoroughly with product and let dry without wiping.
    • For children under 6, use only with adult supervision.
    • Not recommended for use on infants.
  • STORAGE AND HANDLING

    Store 20-25*C (66-77*F)

  • INACTIVE INGREDIENT

    Benzethonium Chloride, Dimethicone, Farnesol, Panthenol, PEG-12, Polyaminopropyl Biguanide, Water.

  • PRINCIPAL DISPLAY PANEL

    Single Wipe Labeling

    NDC: 57362-469-18

    FrontBack

  • INGREDIENTS AND APPEARANCE
    ANTISEPTIC WIPES 
    zylast hand wipes swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57362-469
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL76 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57362-469-1960 mL in 1 PACKAGE; Type 0: Not a Combination Product08/01/2020
    2NDC:57362-469-185 mL in 1 POUCH; Type 0: Not a Combination Product08/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/01/2020
    Labeler - Westwood Laboratories (078363903)
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