Home NDC 0220-2872 KALI CHLORICUM
Product NDC 0220-2872
11-digit product format 002202872
Labeler code 0220
Product ID 0220-2872_3a880519-b150-1eaf-e063-6294a90aaceb
Type HUMAN OTC DRUG
Nonproprietary name POTASSIUM CHLORATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-01-01
Substance POTASSIUM CHLORATE
Active strength 200 [kp_C]/200[kp_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 Additional Listing Data#
Finished product Yes
Brand name base KALI CHLORICUM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM CHLORATE 200 [kp_C]/200[kp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H35KS68EE7 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 0220-2872-41 KALI CHLORICUM 200 [kp_C] in 1 TUBE PELLET 200 1
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 Sample Exclude flag Status 0220-2872-41 00220287241 200 [kp_C] in 1 TUBE (0220-2872-41) 2025-01-01 No No Current