FDA.reportPublic FDA data

Povidone Iodine Prep Pad

Manufacturer
NINGBO TIANBO FIRST AID PRODUCT CO., LTD. | Lights Medical Manufacture Co., Ltd.
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:32:37

Label at a glance#

ProductPovidone Iodine Prep Pad
Active ingredientPOVIDONE-IODINE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Povidone-Iodine USP (10%)

OTC - PURPOSE SECTION

Purpose: Antiseptic

INDICATIONS & USAGE SECTION

Use:

First aid antiseptic to help prevent infection in minor cuts, scrapes and burns.

WARNINGS SECTION

Warnings:

For external use only

Do not use if allergic to iodine or in the eyes

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if infection occurs or if redness, irritation, swelling, or pain persists or increases

DOSAGE & ADMINISTRATION SECTION

Apply locally as need

INACTIVE INGREDIENT SECTION

Inactive Ingredient

Citric acid, purified water, Sodium phosphate dibasic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73288-002-012023-03-01C16284748780-1ba0f9c33-473a-a910-e053-dadaa90a0b8573288-002
73288-002-012023-01-30C16284748780-1ba0f9c33-473a-a910-e053-dadaa90a0b8573288-002
73288-002-012021-04-28C16284748780-1ba0f9c33-473a-a910-e053-dadaa90a0b8573288-002
73288-002-012021-01-29C16284748780-1ba0f9c33-473a-a910-e053-dadaa90a0b8573288-002

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73288-002-01Povidone Iodine Prep Pad0.67 g in 1 PATCHSOLUTION0.676
73288-002-01Povidone Iodine Prep Pad2 in 1 PACKETSOLUTION26

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73288-00273288-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM PHOSPHATE, DIBASICGR686LBA74IACT
POVIDONE-IODINE85H0HZU99MACTIM
WATER059QF0KO0RIACT

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 Prep PadPOVIDONE-IODINENINGBO TIANBO FIRST AID PRODUCT CO., LTD.6d472aef-0d95-4c21-a373-bd16bc7b63ed2026-01-12WarningsExact identifier
ndc (package): 73288-002-01
ndc (product): 73288-002
ndc11 (package): 73288000201
spl id: 483a2b59-9a62-dbf5-e063-6394a90a671e
spl set id: 6d472aef-0d95-4c21-a373-bd16bc7b63ed

Reported adverse events (FAERS/openFDA)#

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