FDA.reportPublic FDA data

Povidone Iodine Pad

Product NDC
59050-705
11-digit product format
590500705
Labeler code
59050
Product ID
59050-705_276b2979-694a-5726-e063-6394a90a7c65
Type
HUMAN OTC DRUG
Nonproprietary name
POVIDONE-IODINE
Dosage form
LIQUID
Route
TOPICAL
Labeler
Changzhou Maokang Medical Products Co., Ltd
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-05-30
Substance
POVIDONE-IODINE
Active strength
100 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Povidone Iodine Pad
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
POVIDONE-IODINE100 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
85H0HZU99MInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
797730Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1936c438-9de6-928a-e063-6394a90ae2f1Available on FDA.report

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

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 (product): 59050-705

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
797730povidone-iodine 10 % Medicated PadPSN1936c438-9de6-928a-e063-6394a90ae2f13
797730povidone-iodine 100 MG/ML Medicated PadSCD1936c438-9de6-928a-e063-6394a90ae2f13
797730povidone-iodine 10 % (titratable iodine 1 % ) Medicated PadSY1936c438-9de6-928a-e063-6394a90ae2f13
797730povidone-iodine 10 % Medicated PadSY1936c438-9de6-928a-e063-6394a90ae2f13
797730povidone-iodine 10 % Medicated SwabstickSY1936c438-9de6-928a-e063-6394a90ae2f13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
59050-705-0159050070501.5 g in 1 POUCH (59050-705-01) 2024-05-30NoNoCurrent