Home NDC 68786-132 Povidone Iodine Prep
Product NDC 68786-132
11-digit product format 687860132
Labeler code 68786
Product ID 68786-132_3e014f0c-43e0-482e-e063-6294a90a44ce
Type HUMAN OTC DRUG
Nonproprietary name Povidone Iodine
Dosage form SOLUTION
Route TOPICAL
Labeler Sion Biotext Medical Ltd
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-07-16
Substance POVIDONE-IODINE
Active strength 1 g/100mL
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 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2021-12-27 23:28 UTC · source 2021-12-27 excluded product product 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 68786-132-01 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 68786-132-01 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 68786-132-01 9bebd1f3094a…5416666fcb17…
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 Prep
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POVIDONE-IODINE 1 g/100mL
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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68786-132-01 Povidone Iodine Prep 22.18 mL in 1 PACKET SOLUTION 22.18 5 68786-132-01 Povidone Iodine Prep 500 in 1 CASE SOLUTION 500 5 68786-132-02 Povidone Iodine Prep 100 in 1 CASE SOLUTION 100 5 68786-132-02 Povidone Iodine Prep 22.18 mL in 1 PACKET SOLUTION 22.18 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68786-132 POVIDONE IODINE PREP (POVIDONE IODINE) SOLUTION [SION BIOTEXT MEDICAL LTD] 4 Current NDC, Legacy NDC, 4 package rows 20240125_e05af551-647d-4278-bb7f-86f888ddbb8b.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 85 of 114 · 2,277 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 68786-132-01 68786013201 500 PACKET in 1 CASE (68786-132-01) / 22.18 mL in 1 PACKET 500 packet 2015-07-16 0000-00-00 No No Current 68786-132-02 68786013202 100 PACKET in 1 CASE (68786-132-02) / 22.18 mL in 1 PACKET 100 packet 2015-07-16 No No Current