Label: PRO-LINK PROFORMANCE FOAMING ANTIMICROBIAL SP- chloroxylenol liquid

  • NDC Code(s): 66908-083-42, 66908-083-67
  • Packager: Pro-Link, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 17, 2024

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 productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor ifirritation 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 product and thoroughly cover hands with lather
    • Rinse well and dry hands completely
  • Inactive ingredients

    Water (Aqua), Alcohol, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Propylene Glycol, Ammonium Xylenesulfonate, Cocamide MEA, Glycerin, Isopropyl Alcohol, Lactic Acid, Retinyl Palmitate, Simmondsia Chinensis (Jojoba) Seed Oil, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Ammonium Sulfate, Fragrance (Parfum), Methylchloroisothiazolinone, Methylisothiazolinone, Red 4 (CI 14700), Yellow 6 (CI 15985)

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    PRO-LINK PROFORMANCE FOAMING ANTIMICROBIAL SP 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66908-083
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    JOJOBA OIL (UNII: 724GKU717M)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    CORN OIL (UNII: 8470G57WFM)  
    AMMONIUM SULFATE (UNII: SU46BAM238)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66908-083-421250 mL in 1 PACKAGE; Type 0: Not a Combination Product08/28/2023
    2NDC:66908-083-672000 mL in 1 PACKAGE; Type 0: Not a Combination Product08/28/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/28/2023
    Labeler - Pro-Link, Inc. (144650637)
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!