BM Kali Mur (kali muriaticum) NDC 82969-1105

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-1105Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-1105Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
82969-1105-1	82969110501	30000 mg in 1 BOTTLE, GLASS (82969-1105-1)Marketed from Jan 1, 2015
82969-1105-2	82969110502	500000 mg in 1 JAR (82969-1105-2)Marketed from Jan 1, 2015

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): BM Kali Mur
Generic name (nonproprietary): kali muriaticum
Active ingredients: Potassium chloride — 6 [hp_X]/60mg
Dosage form: Tablet
Route: Oral
Labeler: Total Operations Management LLC DBA:Bestmade Natural Products Micro
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2027
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 82969-1105_53ba9fb6-322f-8056-e063-6394a90a9f30SPL ID 53ba9fb6-322f-8056-e063-6394a90a9f30SPL set ID 53ba82f3-be9f-51d7-e063-6394a90a877dUNII 660YQ98I10
Pharmacologic class: Osmotic Laxative; Potassium Salt

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N482969110501 followed by a unit qualifier and the quantity

Package 82969-1105-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jun 8, 2026.

Indications (excerpt from the label)

Helps temporarily relieve: occasional dry cough; sneezing; ear blockage; mild body aches; swollen glands; sore throat; runny nose with light-colored discharge.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)