Home NDC 0220-0644-41 Aurum muriaticum kalinatum
Product NDC 0220-0644
Requested package NDC 0220-0644-41
11-digit product format 002200644
Labeler code 0220
Product ID 0220-0644_09ac80f8-325d-a443-e063-6394a90a1438
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name POTASSIUM TETRACHLOROAURATE DIHYDRATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance POTASSIUM TETRACHLOROAURATE DIHYDRATE
Active strength 9 [hp_C]/9[hp_C]
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 Aurum muriaticum kalinatum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM TETRACHLOROAURATE DIHYDRATE 9 [hp_C]/9[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SYJ0T39LVU Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-0644-41 Aurum muriaticum kalinatum 9 [hp_C] in 1 TUBE PELLET 9 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-0644 AURUM MURIATICUM KALINATUM (POTASSIUM TETRACHLOROAURATE DIHYDRATE ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20231109_84749c71-5f3c-2dda-e053-2991aa0aed8d.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 0220-0644-41 00220064441 9 [hp_C] in 1 TUBE (0220-0644-41) 1983-03-03 0000-00-00 No No Current