Label: POVIDONE IODINE- povidone-iodine swab

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 30, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active Ingredient

    Povidone Iodine 10%

  • Purpose

    Antiseptic

  • Uses:

    • First aid to help prevent skin infection in minor cuts, scrapes, and burns
    • Patient preoperative skin preparation: Helps to reduce bacteria that potentially can cause skin infection.

  • Warnings:

    For external use only.

  • Do not use:

    • In the eyes
    • Longer than one week unless directed by a doctor
    • On individuals who are allergic or sensitive to iodine
    • Or apply over large areas of the body
  • Ask a doctor before use if you have:

    • Deep or puncture wounds
    • Animal bites
    • Serious wounds
  • Stop use and ask a doctor if:

    • Irritation and redness develops
    • If condition persists for more than 72 hours, consult a physician.


  • Keep out of reach of children:

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

  • Directions:

    Tear at notch. Remove applicator. Discard applicator after single use.

    As a first aid antispetic:

    • Clean affected area
    • Apply 1-3 times daily
    • May be covered with a sterile bandage
    • If bandaged, let dry first.

    For preoperative patient skin preparation

    • Clean area
    • Apply to operative site prior to surgery using applicator.

  • Other Information:

    • Store at room temperature
    • Avoid excessive heat
  • Inactive Ingredients

    Citric Acid, Glycerin, Polysorbate 80 (Tween 80), Sodium Citrate UPS, Sodium Phosphate Dibasic, Water

  • Principal Display Panel

    PROCURE

    HEALTHCARE PRODUCTS

    POVIDONE

    IODINE

    PREP PAD

    Antiseptic

    100 PADS

    123

  • INGREDIENTS AND APPEARANCE
    POVIDONE IODINE 
    povidone-iodine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55681-751
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE0.1 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55681-751-0010 in 1 CASE05/25/2023
    1100 in 1 BOX
    10.1 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/25/2023
    Labeler - TwinMed LLC (009579330)
    Registrant - TwinMed LLC (009579330)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sion Biotext Mexico SAPI de CV951575186manufacture(55681-751)
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

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!