Povidone Iodine

Manufacturer
Sion Biotext Medical Ltd | Sion Biotext Mexico SAPI de CV
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
monthly-update
Hydrated at
2026-06-03 17:52:32

Label at a glance#

ProductPovidone Iodine
Active ingredientPOVIDONE-IODINE
Label structure12 sections

Indications and uses

Antiseptic cleanser to help prevent infection in minor cuts, scrapes and burns. For preparation of the skin prior to surgery. Helps reduce bacteria that can potentially cause skin infection.

Dosage and administration

Tear at notch Remove applicator Use only once 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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Povidone Iodine 10%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Antiseptic cleanser to help prevent infection in minor cuts, scrapes and burns.
  • For preparation of the skin prior to surgery.
  • Helps reduce bacteria that can potentially cause skin infection.

Warnings

WARNINGS SECTION

For External Use Only.

Do not use

OTC - DO NOT USE SECTION

  • In the eyes
  • As a first aid antiseptic for longer than 1 week
  • Over large areas of the body

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • Deep or puncture wounds
  • Animal bites
  • Serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Condition worsens or persists for more than 72 hours
  • Irritation and redness develops

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Tear at notch
  • Remove applicator
  • Use only once

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

OTHER SAFETY INFORMATION

  • Store at room temperature
  • Avoid excessive heat

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Nonoxynol-9, water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 Medium

Povidone-Iodine

Prep pads

Antispetic/Germicide

For External Use Only

Sion Biotext

Medical Ltd.

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797730povidone-iodine 10 % Medicated PadPSN6
797730povidone-iodine 100 MG/ML Medicated PadSCD6
797730povidone-iodine 10 % (titratable iodine 1 % ) Medicated PadSY6
797730povidone-iodine 10 % Medicated PadSY6
797730povidone-iodine 10 % Medicated SwabstickSY6

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68786-140-01Povidone Iodine10 in 1 CASESWAB106
68786-140-01Povidone Iodine100 in 1 BOXSWAB1006

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
POVIDONE-IODINEACTIVE INGREDIENT85H0HZU99M1
IODINEACTIVE MOIETY9679TC07X41
NONOXYNOL-9INACTIVE INGREDIENT48Q180SH9T1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68786-14068786-140-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POVIDONE-IODINE85H0HZU99MACTIM
NONOXYNOL-948Q180SH9TIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52024-01-24full-release2026-06-01 00:07:49

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
NONOXYNOL-9NONOXYNOL-948Q180SH9TCLOTH / TOPICALNAExact identifier — unii+route
2 equally ranked IID candidates
NONOXYNOL-9NONOXYNOL-948Q180SH9TCLOTH / TOPICALNAExact identifier — unii+route
2 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Povidone IodinePOVIDONE-IODINESion Biotext Medical Ltd3ef9a05b-e434-4f6d-94a1-94aa6723fe8f2026-01-08WarningsExact identifier
ndc (package): 68786-140-01
ndc (product): 68786-140
ndc11 (package): 68786014001
spl id: 47e7d21f-e345-6413-e063-6294a90aa9be
spl set id: 3ef9a05b-e434-4f6d-94a1-94aa6723fe8f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.