Povidone Iodine Pad

Manufacturer
Changzhou Maokang Medical Products Co., Ltd
Effective date
2024-11-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:38:13

Label at a glance#

ProductPovidone Iodine Pad
Active ingredientPOVIDONE-IODINE
Label structure7 sections

Dosage and administration

Clean area. Apply to the operative site prior to surgery.

Label contents#

Full prescribing information#

Active Ingredient 

OTC - ACTIVE INGREDIENT SECTION

Povidone-Iodine 10%w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For preparation of the skin prior to surgery

Warnings

WARNINGS SECTION

For external use only.

Do not apply to persons allergic to iodine.

Do not use

OTC - DO NOT USE SECTION

in the eyes.

Ask a doctor before use 

OTC - ASK DOCTOR SECTION

if injuries are deep wounds, puncture wound, serious burns.

• Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed or gets in eyes, get medical help, or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean area. Apply to the operative site prior to surgery.

Other Information

SPL UNCLASSIFIED SECTION

1% titratable iodine. Store at ambient temperatures.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Hydroxyethyl cellulose, nonoxynol-10, alkyl glucoside, potassium iodide, sodium hydroxide, glycerin, citric acid, purified water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label12Label12

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797730povidone-iodine 10 % Medicated PadPSN3
797730povidone-iodine 100 MG/ML Medicated PadSCD3
797730povidone-iodine 10 % (titratable iodine 1 % ) Medicated PadSY3
797730povidone-iodine 10 % Medicated PadSY3
797730povidone-iodine 10 % Medicated SwabstickSY3

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59050-705-01Povidone Iodine Pad0.5 g in 1 POUCHLIQUID0.53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59050-705POVIDONE IODINE PAD (POVIDONE-IODINE) LIQUID [CHANGZHOU MAOKANG MEDICAL PRODUCTS CO., LTD]3Current NDC, 1 package rows20241122_1936c438-9de6-928a-e063-6394a90ae2f1.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59050-70559050-705-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

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 Iodine PadPOVIDONE-IODINEChangzhou Maokang Medical Products Co., Ltd1936c438-9de6-928a-e063-6394a90ae2f12024-11-21WarningsExact identifier
ndc (package): 59050-705-01
ndc (product): 59050-705
ndc11 (package): 59050070501
spl id: 276b2979-694a-5726-e063-6394a90a7c65
spl set id: 1936c438-9de6-928a-e063-6394a90ae2f1

Reported adverse events (FAERS/openFDA)#

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