Label: CLEAN WORKS- peracetic acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated April 30, 2020

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

View All Sections
  • Active Ingredient

    Peracetic Acid 0.125%

  • Purpose

    Antiseptic

  • Use

    utensils, etc. Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warning

    Be careful not to drink

  • Do not use

    In children less than 2 months of age

    On open skin wounds

  • When using this product

    keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thorough with water.

  • Stop use and ask a doctor

    if irritation or rash occurs. These may by signs of a serious condition.

  • Keep out of reach of children.

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

  • Directions

    Watch for children under 6 years of age to avoid spraying, rubbing, rubbing them on their backs, or drinking this product.

  • Inactive ingredients

    Water, Thuja Oil

  • Package Label

    520ml NDC: 77166-201-01 Label

  • INGREDIENTS AND APPEARANCE
    CLEAN WORKS 
    peracetic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77166-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PERACETIC ACID (UNII: I6KPI2E1HD) (PERACETIC ACID - UNII:I6KPI2E1HD) PERACETIC ACID0.125 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CEDAR LEAF OIL (UNII: BJ169U4NLG)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77166-201-01520 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/07/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/07/2020
    Labeler - SOYSKOREA CO., LTD (694764255)
    Registrant - SOYSKOREA CO., LTD (694764255)
    Establishment
    NameAddressID/FEIBusiness Operations
    SOYSKOREA CO., LTD694764255manufacture(77166-201)
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!