Home NDC 81526-002 TM Titus Medical Povidone Iodine
Product NDC 81526-002
11-digit product format 815260002
Labeler code 81526
Product ID 81526-002_2be150f0-1de0-7377-e063-6394a90a4f13
Type HUMAN OTC DRUG
Nonproprietary name POVIDONE-IODINE
Dosage form OINTMENT
Route TOPICAL
Labeler Titus Medical LLC
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-06-21
Substance POVIDONE-IODINE
Active strength 1 g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 81526-002 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 81526-002 81526-002-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 TM Titus Medical Povidone Iodine
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POVIDONE-IODINE 1 g/100g
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 312563 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81526-002-01 TM Titus Medical Povidone Iodine 100 in 1 BOX OINTMENT 100 5 81526-002-01 TM Titus Medical Povidone Iodine 1 g in 1 POUCH OINTMENT 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81526-002 TM TITUS MEDICAL POVIDONE IODINE (POVIDONE-IODINE) OINTMENT [TITUS MEDICAL LLC] 5 Current NDC, Legacy NDC, 2 package rows 20250119_af7840c0-239e-4ff6-8d27-614e7d71ca99.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 9 of 115 · 2,286 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81526-002-01 81526000201 100 POUCH in 1 BOX (81526-002-01) / 1 g in 1 POUCH 100 pouch 2021-06-21 0000-00-00 No No Current