Home NDC 85816-1031 BM Potassium dichromate (Kali Dichrom)
Product NDC 85816-1031
11-digit product format 858161031
Labeler code 85816
Product ID 85816-1031_44fb9799-1c7a-b042-e063-6394a90a9aec
Type HUMAN OTC DRUG
Nonproprietary name Potassium Dichromate
Dosage form TABLET
Route ORAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-06-01
Substance POTASSIUM DICHROMATE
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 dichromate (Kali Dichrom)
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM DICHROMATE 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 T4423S18FM 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 85816-1031-1 BM Potassium dichromate (Kali Dichrom) 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 85816-1031-1 85816103101 30000 mg in 1 BOTTLE, GLASS (85816-1031-1) 30000 mg 2025-06-01 No No Current