Home NDC 37662-0887-3 Kali Muriaticum
Product NDC 37662-0887
Requested package NDC 37662-0887-3
11-digit product format 376620887
Labeler code 37662
Product ID 37662-0887_e3c8e13d-a67e-162c-e053-2a95a90abd11
Type HUMAN OTC DRUG
Nonproprietary name Kali Muriaticum
Dosage form PELLET
Route ORAL
Labeler Hahnemann Laboratories, INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-07-14
Substance POTASSIUM CHLORIDE
Active strength 200 [hp_C]/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 Additional Listing Data#
Finished product Yes
Brand name base Kali Muriaticum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM CHLORIDE 200 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 660YQ98I10 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 37662-0887-1 Kali Muriaticum 200 in 1 VIAL, GLASS PELLET 200 1 37662-0887-2 Kali Muriaticum 500 in 1 VIAL, GLASS PELLET 500 1 37662-0887-3 Kali Muriaticum 3000 in 1 BOTTLE, GLASS PELLET 3000 1 37662-0887-4 Kali Muriaticum 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 37662-0887 KALI MURIATICUM PELLET [HAHNEMANN LABORATORIES, INC.] 1 Current NDC, Legacy NDC, 4 package rows 20220716_e3c8e13d-a67d-162c-e053-2a95a90abd11.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 37662-0887-3 37662088703 3000 PELLET in 1 BOTTLE, GLASS (37662-0887-3) 3000 pellet 2022-07-14 0000-00-00 No No Current