Label: HEALTHCARE ANTISEPTIC TOWELETTE- chloroxylenol liquid

  • 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 December 27, 2017

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

View All Sections
  • Healthcare Antiseptic Towelette


  • ACTIVE INGREDIENT

    Chloroxylenol 0.5%

    Antiseptic

  • Uses:

    • For handwashing to decrease bacteria on the skin
    • Helps prevent cross contamination by hand contact
    • Helps prevent drying and chafing of skin
    • Recommended for repeated use
  • Warnings:

    For external use only.

    When using this product

    • Do not use in or near eyes
    • Use in a well-ventilated area
    • Discontinue use if irritation and redness develop

    Keep out of reach of children.

    In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

  • Directions

    • Open packet and remove towelette
    • Wipe hands thoroughly with towelette
    • Rinse thoroughly and dry
  • Other Information

    • Store at room temperature
    • For Hospital and Professional Use Only
  • Inactive Ingredients

    • Dimethicone Copolyol, Fragrance, Isopropyl C 12-15 Pareth-9 Carboxylate, Nonoxynol-9, SD Alcohol 40 (10%) and Water
  • Healthcare Antiseptic Towelette 1 Count (44019-401-00)

    Healthcare antiseptic Towelette

  • INGREDIENTS AND APPEARANCE
    HEALTHCARE ANTISEPTIC TOWELETTE 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44019-401
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    C12-15 PARETH-9 (UNII: H3ZIY6WP1R)  
    NONOXYNOL-9 (UNII: 48Q180SH9T)  
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44019-401-001.6 g in 1 PACKET; Type 0: Not a Combination Product08/03/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/03/2016
    Labeler - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)
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!