Home NDC 37662-2243-2 Kali Ferrocyanatum
Product NDC 37662-2243
Requested package NDC 37662-2243-2
11-digit product format 376622243
Labeler code 37662
Product ID 37662-2243_f176bba9-acef-ccc0-e053-2a95a90aa506
Type HUMAN OTC DRUG
Nonproprietary name Kali Ferrocyanatum
Dosage form PELLET
Route ORAL
Labeler Hahnemann Laboratories, INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-01-04
Substance POTASSIUM FERROCYANIDE TRIHYDRATE
Active strength 1 [hp_M]/1
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 Kali Ferrocyanatum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM FERROCYANIDE TRIHYDRATE 1 [hp_M]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 961WP42S65 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37662-2243-1 Kali Ferrocyanatum 200 in 1 VIAL, GLASS PELLET 200 1 37662-2243-2 Kali Ferrocyanatum 500 in 1 VIAL, GLASS PELLET 500 1 37662-2243-3 Kali Ferrocyanatum 3000 in 1 BOTTLE, GLASS PELLET 3000 1 37662-2243-4 Kali Ferrocyanatum 10000 in 1 BOTTLE, GLASS PELLET 10000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37662-2243 KALI FERROCYANATUM PELLET [HAHNEMANN LABORATORIES, INC.] 1 Current NDC, Legacy NDC, 4 package rows 20230106_f176bba9-acee-ccc0-e053-2a95a90aa506.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 Units Marketing start Marketing end Sample Exclude flag Status 37662-2243-2 37662224302 500 PELLET in 1 VIAL, GLASS (37662-2243-2) 500 pellet 2023-01-04 0000-00-00 No No Current