FDA.reportPublic FDA data

Povidone-Iodine Prep Pad

Manufacturer
Nantong Furuida Packaging Products Co., Ltd.
Effective date
2021-05-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:40:30

Label at a glance#

ProductPovidone-Iodine Prep Pad
Active ingredientPOVIDONE-IODINE
Label structure6 sections

Dosage and administration

Apple locally as needed.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

POVIDONE-IODINE 10% W/v (equivalent to iodine 1%)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

For External use only.
Discontinue use if irritation and redness develop

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

Apple locally as needed.

Other information

SPL UNCLASSIFIED SECTION

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

Use

INDICATIONS & USAGE SECTION

Antiseptic for preparation of the skin

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797730povidone-iodine 10 % Medicated PadPSN2
797730povidone-iodine 100 MG/ML Medicated PadSCD2
797730povidone-iodine 10 % (titratable iodine 1 % ) Medicated PadSY2
797730povidone-iodine 10 % Medicated PadSY2
797730povidone-iodine 10 % Medicated SwabstickSY2

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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73118-001-012024-01-30C16284748780-1ba0f9c33-3b1f-a910-e053-dadaa90a0b85731180--001
73118-001-012021-05-24C16284748780-1ba0f9c33-3b1f-a910-e053-dadaa90a0b85731180--001
73118-001-012021-01-29C16284748780-1ba0f9c33-3b1f-a910-e053-dadaa90a0b85731180--001

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73118-001-01Povidone-Iodine Prep Pad1 in 1 PACKAGESWAB12
73118-001-01Povidone-Iodine Prep Pad200 in 1 BOXSWAB2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73118-001POVIDONE-IODINE PREP PAD (POVIDONE-IODINE) SWAB [NANTONG FURUIDA PACKAGING PRODUCTS CO., LTD.]2Legacy NDC, 2 package rows20210525_89dd9032-b522-69a2-e053-2a95a90a3336.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73118-00173118-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
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
c3142d05-1b79-b4ba-e053-2995a90af90a89dd9032-b522-69a2-e053-2a95a90a33362021-05-24WarningsExact identifier
spl id: c3142d05-1b79-b4ba-e053-2995a90af90a
spl set id: 89dd9032-b522-69a2-e053-2a95a90a3336

Reported adverse events (FAERS/openFDA)#

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