Home NDC 85816-1033 BM Potassium iodide (Kali Iod) 6X
Product NDC 85816-1033
11-digit product format 858161033
Labeler code 85816
Product ID 85816-1033_44fbad1f-e864-c63c-e063-6394a90a8b83
Type HUMAN OTC DRUG
Nonproprietary name BM Potassium iodide (Kali Iod)
Dosage form TABLET
Route ORAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-06-01
Substance POTASSIUM IODIDE
Active strength 6 [hp_X]/60mg
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base BM Potassium iodide (Kali Iod) 6X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM IODIDE 6 [hp_X]/60mg
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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85816-1033-1 BM Potassium iodide (Kali Iod) 6X 30000 mg in 1 BOTTLE, GLASS TABLET 30000 2
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 85816-1033-1 85816103301 30000 mg in 1 BOTTLE, GLASS (85816-1033-1) 30000 mg 2025-06-01 No No Current