Home NDC 62106-1054 KALIUM MURIATICUM 6X
Product NDC 62106-1054
11-digit product format 621061054
Labeler code 62106
Product ID 62106-1054_e33c6585-d77e-0547-e053-2a95a90ad493
Type HUMAN OTC DRUG
Nonproprietary name Potassium Chloride
Dosage form TABLET
Route SUBLINGUAL
Labeler Seroyal USA
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-10-23
Substance POTASSIUM CHLORIDE
Active strength 6 [hp_X]/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 KALIUM MURIATICUM 6X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM CHLORIDE 6 [hp_X]/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 62106-1054-2 KALIUM MURIATICUM 6X 100 in 1 BOTTLE, GLASS TABLET 100 7 62106-1054-2 KALIUM MURIATICUM 6X 1 in 1 CARTON TABLET 1 7
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62106-1054 KALIUM MURIATICUM 6X (POTASSIUM CHLORIDE) TABLET [SEROYAL USA] 7 Current NDC, Legacy NDC, 2 package rows 20220709_22c95b6a-dd5d-476e-e054-00144ff8d46c.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 62106-1054-2 62106105402 1 BOTTLE, GLASS in 1 CARTON (62106-1054-2) / 100 TABLET in 1 BOTTLE, GLASS 2015-10-23 0000-00-00 No No Current