Bm Bm38 Drops NDC 82969-2338

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-2338Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-2338Add 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
82969-2338-1	82969233801	30 mL in 1 BOTTLE, GLASS (82969-2338-1)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): Bm Bm38 Drops
Generic name (nonproprietary): berb aqui, graphite, hydrocotyle, kali brom, kali iodat, natrum phos, sulphur iodat
Active ingredients: Sulfur iodide — 7 [hp_X]/mLPotassium iodide — 7 [hp_X]/mLPotassium bromide — 7 [hp_X]/mLGraphite — 18 [hp_X]/mLSodium phosphate, Dibasic, Heptahydrate — 12 [hp_X]/mLBerberis aquifolium root bark — 2 [hp_X]/mLCentella asiatica whole — 2 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Total Operations Management LLC DBA:Bestmade Natural Products Micro
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2027
Identifiers: Product ID 82969-2338_5410afaa-6b81-f7e1-e063-6294a90a8706SPL ID 5410afaa-6b81-f7e1-e063-6294a90a8706SPL set ID 5410af95-519a-f0d5-e063-6294a90ac0cfUNII L6L8KA2AA0, 1C4QK22F9J, OSD78555ZM, 4QQN74LH4O, 70WT22SF4B, VZJ9F3C3SB, 7M867G6T1U

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

N482969233801 followed by a unit qualifier and the quantity

Package 82969-2338-01. 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 Jun 12, 2026.

Indications (excerpt from the label)

Uses* Helps temporarily relieve: pimples, skin redness, itching, irritation, oily skin, and clogged pores.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)