Bestmade Natural Products BM182 Pellets NDC 82969-7182

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-7182Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-7182Add 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
82969-7182-1	82969718201	30 [hp_C] in 1 BOTTLE, GLASS (82969-7182-1)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 BM182 Pellets
Generic name (nonproprietary): graphites, hepar sulf, merc sol, muriatic acid
Active ingredients: Graphite — 30 [hp_C]/30[hp_C]Calcium sulfide — 30 [hp_C]/30[hp_C]Mercurius solubilis — 30 [hp_C]/30[hp_C]Hydrochloric acid — 30 [hp_C]/30[hp_C]
Dosage form: Tablet, Soluble
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 82969-7182_3242e013-2953-2b56-e063-6294a90a1693SPL ID 3242e013-2953-2b56-e063-6294a90a1693SPL set ID 3242e013-2952-2b56-e063-6294a90a1693UNII 4QQN74LH4O, 1MBW07J51Q, 324Y4038G2, QTT17582CB

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

N482969718201 followed by a unit qualifier and the quantity

Package 82969-7182-01. 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 Apr 8, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves occasional skin discomfort and irritation associated with skin bumps with or without pus.* *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE. NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED. This product is not intended to diagnose, treat, cure, or prevent any disease.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)