BM Nat Mur Icing Sugar (natrum muriaticum icing sugar) NDC 82969-1121

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-1121Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-1121Add 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
82969-1121-1	82969112101	30000 mg in 1 BOTTLE, GLASS (82969-1121-1)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 Nat Mur Icing Sugar
Generic name (nonproprietary): natrum muriaticum icing sugar
Active ingredients: Sodium 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
Identifiers: Product ID 82969-1121_5356d3a7-fb25-d51e-e063-6394a90a9e8aSPL ID 5356d3a7-fb25-d51e-e063-6394a90a9e8aSPL set ID 5356d350-1325-7299-e063-6294a90a96a0UNII 451W47IQ8X

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

N482969112101 followed by a unit qualifier and the quantity

Package 82969-1121-01. 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 3, 2026.

Indications (excerpt from the label)

Uses* Helps temporarily relieve: imbalances related to dryness or excess moisture; loose stools, runny nose, vomiting, and painful urination; feelings of heaviness, coldness, fatigue, headaches, and weakness; and skin-related concerns.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)