Home NDC 0904-7639 Povidone-Iodine
Product NDC 0904-7639
11-digit product format 009047639
Labeler code 0904
Product ID 0904-7639_59041cb4-9e59-5d10-e063-6394a90a6b07
Type HUMAN OTC DRUG
Nonproprietary name Povidone-Iodine
Dosage form SOLUTION
Route TOPICAL
Labeler Major Pharmaceuticals
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-14
Substance POVIDONE-IODINE
Active strength 100 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
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
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POVIDONE-IODINE 100 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 85H0HZU99M Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 312564 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 44 of 115 · 2,286 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 0904-7639-54 00904763954 237 mL in 1 BOTTLE, PLASTIC (0904-7639-54) 237 ml 2026-08-14 No No Current