Label: MAOKANG MEDICAL 10 POVIDONE IODINE- povidone-iodine solution

  • NDC Code(s): 59050-272-10
  • Packager: Changzhou Maokang Medical Products Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 16, 2024

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

View All Sections
  • Drug Facts

  • Active ingredient

    Povidone-Iodine USP 10%

    Purpose

    Antiseptic

  • Use

    for antiseptic skin preparation

  • Warnings

    Do not use

    • if allergic to Iodine
    • do not use in the eye

    Stop use and ask a doctor if

    • redness,irritation,swelling or pain persists or increases
    • infection occurs

    Keep out of reach of children.

    In case of accidental ingestion,seek professional assistance or consult a poison control center immediately. 

    Avoid pooling beneath patient.

    Ask a doctor before use if injuries are

    • deep or puncture wounds
    • serious burns
  • Directions

    Apply product to skin as needed

  • Other information

    • 1% titratable iodine
    • for hospital or professional use only
  • Inactive ingredients:

    Citric Acid,Alkyl Glucoside,Hydroxyethyl Cellulose,Nonoxynol-10,Glycerin,Sodium Hydroxide,Potassium Iodine,Purified Water.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    MAOKANG MEDICAL 10 POVIDONE IODINE 
    povidone-iodine solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59050-272
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    NONOXYNOL-10 (UNII: K7O76887AP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59050-272-102.12 mL in 1 POUCH; Type 0: Not a Combination Product12/27/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00312/27/2023
    Labeler - Changzhou Maokang Medical Products Co., Ltd (421317073)
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!