Bm100 NDC 82969-2400

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-2400Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-2400Add 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
82969-2400-1	82969240001	30 mL in 1 BOTTLE, GLASS (82969-2400-1)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): Bm100
Generic name (nonproprietary): agraphis nutans, castoreum, formica rufa, lemna minor, sanguinaria nitricum, sticta pul, teucrium marum, thuja
Active ingredients: Formica rufa — 10 [hp_C]/mLThuja occidentalis leafy twig — 30 [hp_C]/mLCastor canadensis scent gland secretion — 40 [hp_C]/mLLemna minor whole — 30 [hp_C]/mLLobaria pulmonaria — 20 [hp_C]/mLHyacinthoides non-scripta whole — 40 [hp_C]/mLTeucrium marum whole — 100 [hp_C]/mL
Dosage form: Liquid
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, 2026
Identifiers: Product ID 82969-2400_3d833ef4-8172-d447-e063-6394a90a21c8SPL ID 3d833ef4-8172-d447-e063-6394a90a21c8SPL set ID 3d833ef4-8171-d447-e063-6394a90a21c8UNII 55H0W83JO5, 1NT28V9397, D0MH91LS9C, 621HHM46SV, D1YM0P5Z2T, 5F658PFU56, 10464S0TAA

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

N482969240001 followed by a unit qualifier and the quantity

Package 82969-2400-01. 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 Aug 29, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves occasional nasal obstruction and discomfort, swelling and irritation of the lining of the nose, sneezing, poor sense of smell and taste, and catarrh.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)