Bestmade Natural Products BM102 NDC 82969-2102

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-2102Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-2102Add 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
82969-2102-1	82969210201	30 [hp_C] in 1 BOTTLE, GLASS (82969-2102-1)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 BM102
Generic name (nonproprietary): belladonna, bufo rana, cuprum met., crocus sat, helonias, cuprum ars
Active ingredients: Copper — 30 [hp_C]/30[hp_C]Bufo bufo cutaneous gland — 30 [hp_C]/30[hp_C]Saffron — 30 [hp_C]/30[hp_C]Cupric arsenite — 30 [hp_C]/30[hp_C]Atropa belladonna — 30 [hp_C]/30[hp_C]Chamaelirium luteum 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
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 82969-2102_2d8ecfc4-ab5e-3641-e063-6294a90ac6b2SPL ID 2d8ecfc4-ab5e-3641-e063-6294a90ac6b2SPL set ID 2d8ecfc4-ab5d-3641-e063-6294a90ac6b2UNII 789U1901C5, Q59QU6N72Q, E849G4X5YJ, SK8L60BCSQ, WQZ3G9PF0H, DQV54Y5H3U
Pharmacologic class: Copper-containing Intrauterine Device

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

N482969210201 followed by a unit qualifier and the quantity

Package 82969-2102-01. 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 7, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves discomfort associated with nervous system disturbances, including changes in behavior, movements, feelings, and levels of consciousness.* *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)