Bestmade Natural Products BM20 NDC 82969-2020

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-2020Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-2020Add 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
82969-2020-1	82969202001	30 [hp_C] in 1 BOTTLE, GLASS (82969-2020-1)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 BM20
Generic name (nonproprietary): baptisia tincd4, echinacead3, euphorbiumd6, galium apard12, rumex c.d3, sarsaprillad6,sulphurd6
Active ingredients: Echinacea angustifolia — 30 [hp_C]/30[hp_C]Rumex crispus root — 30 [hp_C]/30[hp_C]Smilax ornata root — 30 [hp_C]/30[hp_C]Sulfur — 30 [hp_C]/30[hp_C]Galium aparine — 30 [hp_C]/30[hp_C]Baptisia tinctoria root — 30 [hp_C]/30[hp_C]Euphorbia resinifera resin — 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 82969-2020_2c50f013-6e6b-47e2-e063-6294a90a733cSPL ID 2c50f013-6e6b-47e2-e063-6294a90a733cSPL set ID ed09608b-64f0-55cc-e053-2995a90aac28UNII VB06AV5US8, 9N1RM2S62C, 2H1576D5WG, 70FD1KFU70, Z4B6561488, 5EF0HWI5WU, 1TI1O9028K

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

N482969202001 followed by a unit qualifier and the quantity

Package 82969-2020-01. 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 Jan 22, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves discomfort due to pimples, irritation, watery blisters, and swelling in the lymphatic glands. Temporarily supports skin health.* *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)