Home NDC 0220-2805 Kali iodatum
Product NDC 0220-2805
11-digit product format 002202805
Labeler code 0220
Product ID 0220-2805_0a0e1685-b645-7e21-e063-6394a90a5324
Type HUMAN OTC DRUG
Nonproprietary name POTASSIUM IODIDE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance POTASSIUM IODIDE
Active strength 30 [hp_X]/30[hp_X]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Kali iodatum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM IODIDE 30 [hp_X]/30[hp_X]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1C4QK22F9J Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-2805-41 Kali iodatum 30 [hp_X] in 1 TUBE PELLET 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-2805 KALI IODATUM (POTASSIUM IODIDE ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20231114_86080b3d-28c4-ed4a-e053-2a91aa0a51dc.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0220-2805-41 00220280541 30 [hp_X] in 1 TUBE (0220-2805-41) 1983-03-03 0000-00-00 No No Current