Bestmade Natural Products BM213 NDC 82969-2213

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-2213Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-2213Add 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
82969-2213-1	82969221301	30 [hp_C] in 1 BOTTLE, GLASS (82969-2213-1)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 BM213
Generic name (nonproprietary): graphites, rhus tox, natrum sulph, carbo veg, nat phos
Active ingredients: Graphite — 30 [hp_C]/30[hp_C]Toxicodendron pubescens leaf — 30 [hp_C]/30[hp_C]Activated charcoal — 30 [hp_C]/30[hp_C]Sodium sulfate — 30 [hp_C]/30[hp_C]Sodium phosphate, Dibasic, Heptahydrate — 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: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers: Product ID 82969-2213_2f6d9587-7186-7fef-e063-6394a90aa6fdSPL ID 2f6d9587-7186-7fef-e063-6394a90aa6fdSPL set ID 2f6d9587-7185-7fef-e063-6394a90aa6fdUNII 4QQN74LH4O, 6IO182RP7A, 2P3VWU3H10, 0YPR65R21J, 70WT22SF4B
Pharmacologic class: Osmotic Laxative

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

N482969221301 followed by a unit qualifier and the quantity

Package 82969-2213-01. 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 Mar 3, 2025.

Indications (excerpt from the label)

Uses Temporarily supports digestion and nutrient absorption. Temporarily relieves discomfort due to digestive problems, including occasional watery and loose stools, weight loss, slimy stools, bloating, tiredness, acidity, coated tongue, dry and hard stools, indigestion, and pale skin.* *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)