Home NDC 72919-728 Potassium Iodide (Saturated)
Product NDC 72919-728
11-digit product format 729190728
Labeler code 72919
Product ID 72919-728_082eb221-e9d4-4638-b97b-6ef337cd368d
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Potassium Iodide
Dosage form SOLUTION
Route ORAL
Labeler Emerald Therapeutics, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-08-18
Substance POTASSIUM IODIDE
Active strength 1 g/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 Potassium Iodide (Saturated)
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM IODIDE 1 g/mL
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 312541 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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72919-728-30 72919072830 30 mL in 1 BOTTLE, GLASS (72919-728-30) 30 ml 2026-08-18 No No Current