Bestmade Natural Products BM184 NDC 82969-2184

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-2184Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-2184Add 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
82969-2184-1	82969218401	30 [hp_C] in 1 BOTTLE, GLASS (82969-2184-1)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 BM184
Generic name (nonproprietary): benzoic acid, buchu, belladonna, terebinthina, thlapsi b.p, triticum rep
Active ingredients: Benzoic acid — 30 [hp_C]/30[hp_C]Elymus repens root — 30 [hp_C]/30[hp_C]Agathosma crenulata whole — 30 [hp_C]/30[hp_C]Turpentine oil — 30 [hp_C]/30[hp_C]Atropa belladonna — 30 [hp_C]/30[hp_C]Capsella bursa-pastoris whole — 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
Other FDA classes: Ammonium Ion Binding Activity (Mechanism)
Identifiers: Product ID 82969-2184_2e9211e3-0e21-741e-e063-6394a90a4da1SPL ID 2e9211e3-0e21-741e-e063-6394a90a4da1SPL set ID 2e9211e3-0e20-741e-e063-6394a90a4da1UNII 8SKN0B0MIM, 3IXW0F6P8W, B6642J883V, C5H0QJ6V7F, WQZ3G9PF0H, W0X9457M59
Pharmacologic class: Nitrogen Binding Agent

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

N482969218401 followed by a unit qualifier and the quantity

Package 82969-2184-01. 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 20, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves discomfort due to bladder issues and excess uric acid, including occasional involuntary urination, burning sensation in the urethra, uneasiness in the bladder, large amounts of colorless urine, and frequent urination.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)