Bestmade Natural Products BM124 NDC 82969-2124

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-2124Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-2124Add 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
82969-2124-1	82969212401	30 [hp_C] in 1 BOTTLE, GLASS (82969-2124-1)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): Bestmade Natural Products BM124
Generic name (nonproprietary): acid nitric, berberis vulg, lycopodium, ocimum can, pareira brava, rubia tinctor
Active ingredients: Nitric acid — 30 [hp_C]/30[hp_C]Berberis vulgaris root bark — 30 [hp_C]/30[hp_C]Ocimum americanum leaf — 30 [hp_C]/30[hp_C]Lycopodium clavatum spore — 30 [hp_C]/30[hp_C]Rubia tinctorum root — 30 [hp_C]/30[hp_C]Chondrodendron tomentosum root — 30 [hp_C]/30[hp_C]
Dosage form: Liquid
Route: Oral
Labeler: Bestmade Natural Products
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 82969-2124_2dcabf24-c014-ce7e-e063-6294a90a4815SPL ID 2dcabf24-c014-ce7e-e063-6294a90a4815SPL set ID 2dcabf24-c013-ce7e-e063-6294a90a4815UNII 411VRN1TV4, 1TH8Q20J0U, 4EX119B76E, C88X29Y479, 0SVP95L23G, 395A3P448Z

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

N482969212401 followed by a unit qualifier and the quantity

Package 82969-2124-01. 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 Feb 10, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves discomfort related to kidney issues, including occasional sharp discomfort across the back, reddish and grey urine, discomfort in the sacral region coming from the kidney, painful urination, nausea, vomiting, urinary tract discomfort, muscle contractions, and frequent urination.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)