Label: POVIDONE IODINE PREP- povidone iodine swab

  • NDC Code(s): 60913-999-02
  • Packager: PHOENIX HEALTHCARE SOLUTIONS, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 17, 2023

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

View All Sections
  • Active ingredient

    Povidone Iodine USP 10% v/v

  • Purpose

    Antiseptic

  • Uses

    • Health-care antiseptic for preparation of the skin prior to surgery
    • First aid antiseptic to help prevent the risk of skin infection in minor cuts, scrapes and burns
  • Warnings:

    For external use only

    Do not

    • use in the eyes
    • use on individuals who are allergic or sensitive to iodine
    • apply over large areas of the body
    • use as a first aid antiseptic longer than 1 week unless directed by a doctor.

    Discontinue use if irritation and redness develop.

    Consult a doctor in case of

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and consult a doctor

    if the condition persists or gets worse.

    Keep out of reach of children

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


  • Directions:

    For preparation of the skin prior to surgery


    • clean the affected area
    • apply a small amount of this product on the area

    For use as a first aid antiseptic

    • clean the affected area
    • apply a small amount of this product on the area 1-3 times daily
    • may be covered with a sterile bandage
    • if bandaged, let dry first.
  • Other information

    Store at room temperature: 59 o - 86 oF (15 o - 30 oC)

  • Inactive ingredients:

    citric acid, glycerin, Makon 8, purified water, sodium hydroxide

  • Principal Display Panel

    Phoenix Healthcare Solutions LLC

    An Innovative Medical Manufacturer

    NDC 60913-999-02

    200 Individual Pads

    Povidone Iodine Prep Pads

    Medium

    For Individual, Professional and Hospital Use

    Saturated with 10% Povidone Iodine for external use only

    Latex Free

    PIN DOT WOVEN

    Label

  • INGREDIENTS AND APPEARANCE
    POVIDONE IODINE PREP 
    povidone iodine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60913-999
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60913-999-02200 in 1 CARTON02/26/2015
    11 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/26/2015
    Labeler - PHOENIX HEALTHCARE SOLUTIONS, LLC (079146847)
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!