FDA.reportPublic FDA data

Iodine Prep Pad Antiseptic

Manufacturer
Yiwu Ori-Power Medtech Co.,Ltd.
Effective date
2026-01-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:33:44

Label at a glance#

ProductIodine Prep Pad Antiseptic
Active ingredientPOVIDONE-IODINE
Label structure7 sections

Dosage and administration

Tear open packet, use Iodine-saturated pad to cleanse desired skin area. Discard pad appropriately after use.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Povidone Iodine 10% USP.

Purpose

OTC - PURPOSE SECTION

First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

Use

INDICATIONS & USAGE SECTION

Topical Antimicrobial Agent For Wound Disinfection.

Directions

DOSAGE & ADMINISTRATION SECTION

Tear open packet, use Iodine-saturated pad to cleanse desired skin area. Discard pad appropriately after use.

Storage

SPL UNCLASSIFIED SECTION

Store at room temperature 15°C - 30°C (59°F - 86°F).

Warnings

WARNINGS SECTION

Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If pain, irritation, redness, swelling, or infection develops, discontinue use and consult physician.

Keep Out  Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental swallowing, seek medical help and contact poison control immediately.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

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
72459-017-01Iodine Prep Pad Antiseptic0.55 g in 1 POUCHSOLUTION0.553

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72459-01772459-017-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
.BETA.-D-GLUCOPYRANOSEJ4R00M814DIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
NONOXYNOL-10K7O76887APIACT
GLYCERINPDC6A3C0OXIACT
SODIUM HYDROXIDE55X04QC32IIACT
POTASSIUM IODIDE1C4QK22F9JIACT
WATER059QF0KO0RIACT
POVIDONE-IODINE85H0HZU99MACTIM

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
Iodine Prep Pad AntisepticPOVIDONE-IODINEYiwu Ori-Power Medtech Co.,Ltd.0fdded64-4e89-d28c-e063-6394a90a7b8f2026-01-01WarningsExact identifier
ndc (package): 72459-017-01
ndc (product): 72459-017
ndc11 (package): 72459001701
spl id: 48d5a48f-36f5-6ebd-e063-6394a90ab435
spl set id: 0fdded64-4e89-d28c-e063-6394a90a7b8f

Reported adverse events (FAERS/openFDA)#

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