Label: GOJO PCMX E-2 SANITIZING LTN SP- chloroxylenol liquid

  • NDC Code(s): 21749-457-20, 21749-457-37, 21749-457-50, 21749-457-55, view more
    21749-457-80
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 25, 2019

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

View All Sections
  • Active ingredient

    Chloroxylenol 0.3%

  • Purpose

    Antimicrobial

  • Uses

    • Handwash to help decrease bacteria on the skin
    • Recommended for repeated use
  • Warnings

    For external use only

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash appears and lasts

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Wet hands
    • Apply a small amount of product and work into a lather
    • Rinse well and dry hands completely
  • Inactive ingredients

    Water (Aqua), Coconut Acid, Oleic Acid, Sodium Sulfate, Ethanolamine, Cocamide MEA, Coco-Betaine, Propylene Glycol, Tetrasodium EDTA

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    GOJO PCMX E-2 SANITIZING LTN SP 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-457
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.003 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCONUT ACID (UNII: 40U37V505D)  
    OLEIC ACID (UNII: 2UMI9U37CP)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    MONOETHANOLAMINE (UNII: 5KV86114PT)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    Coco-Betaine (UNII: 03DH2IZ3FY)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-457-80800 mL in 1 PACKAGE; Type 0: Not a Combination Product02/25/2019
    2NDC:21749-457-202000 mL in 1 PACKAGE; Type 0: Not a Combination Product02/25/2019
    3NDC:21749-457-505000 mL in 1 PACKAGE; Type 0: Not a Combination Product02/25/2019
    4NDC:21749-457-373780 mL in 1 PACKAGE; Type 0: Not a Combination Product02/25/2019
    5NDC:21749-457-55208000 mL in 1 PACKAGE; Type 0: Not a Combination Product02/25/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E02/25/2019
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534MANUFACTURE(21749-457)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414label(21749-457) , pack(21749-457)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!