Bestmade Natural Products BM168 NDC 82969-2168

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-2168Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-2168Add 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
82969-2168-1	82969216801	30 [hp_C] in 1 BOTTLE, GLASS (82969-2168-1)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 BM168
Generic name (nonproprietary): conium, pilocarpine muriate, kali sil, kali ars, sulphur, nat mur
Active ingredients: Potassium silicate — 30 [hp_C]/30[hp_C]Potassium arsenite anhydrous — 30 [hp_C]/30[hp_C]Sulfur — 30 [hp_C]/30[hp_C]Sodium chloride — 30 [hp_C]/30[hp_C]Pilocarpine hydrochloride — 30 [hp_C]/30[hp_C]Conium maculatum flowering top — 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: Cholinergic Agonists (Mechanism)Cholinergic Muscarinic Agonists (Mechanism)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 82969-2168_2e7bc230-8a38-9975-e063-6294a90a15e7SPL ID 2e7bc230-8a38-9975-e063-6294a90a15e7SPL set ID 2e7bc230-8a37-9975-e063-6294a90a15e7UNII J86L1GUL6K, BM2U42PAKI, 70FD1KFU70, 451W47IQ8X, 0WW6D218XJ, Q28R5GF371
Pharmacologic class: Cholinergic Receptor Agonist; Osmotic Laxative; Potassium Salt

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

N482969216801 followed by a unit qualifier and the quantity

Package 82969-2168-01. 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 19, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves occasional throat swelling, elevated body temperature, headaches, loss of appetite, discomfort in the parotid glands, stiff neck, nausea, vomiting, dry mouth, and discomfort when swallowing, talking, chewing, or drinking acidic beverages.* *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)