Bestmade Natural Products BM212 NDC 82969-2212

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-2212Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-2212Add 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
82969-2212-1	82969221201	30 [hp_C] in 1 BOTTLE, GLASS (82969-2212-1)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 BM212
Generic name (nonproprietary): ars alb, kali phos, nat carb, nitric acid
Active ingredients: Potassium phosphate, Dibasic — 30 [hp_C]/30[hp_C]Arsenic trioxide — 30 [hp_C]/30[hp_C]Sodium carbonate — 30 [hp_C]/30[hp_C]Nitric acid — 30 [hp_C]/30[hp_C]
Dosage form: Liquid
Route: Oral
Labeler: Bestmade Natural Products
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 82969-2212_2f37416e-b3b0-f980-e063-6294a90a6be1SPL ID 2f37416e-b3b0-f980-e063-6294a90a6be1SPL set ID 2f37416e-b3af-f980-e063-6294a90a6be1UNII CI71S98N1Z, S7V92P67HO, 45P3261C7T, 411VRN1TV4

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

N482969221201 followed by a unit qualifier and the quantity

Package 82969-2212-01. 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 28, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves occasional fear of illness, obsession, desire to stay warm, extreme sensitivity to cold, debility, mental hopelessness, despair of recovery, self-harm thoughts, irritability, sensitivity to noise, nervousness, breathlessness during a thunderstorm, feeling drowsy during the day, and feeling hysterical with night terrors.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)