Bm Bm13 Drops NDC 85816-2013

NDC codes

FDA NDC Directory

Product NDC (as listed)85816-2013Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85816-2013Add 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
85816-2013-1	85816201301	30 mL in 1 BOTTLE, GLASS (85816-2013-1)Marketed from Jan 1, 2015
85816-2013-2	85816201302	500 mL in 1 JAR (85816-2013-2)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 Bm13 Drops
Generic name (nonproprietary): belladonna, cuprum aceticum, drosera, grindelia, ipecac, lobelia inflata, naphthalinum, yerba santa
Active ingredients: Atropa belladonna — 4 [hp_X]/mLDrosera rotundifolia whole — 3 [hp_X]/mLNaphthalene — 12 [hp_X]/mLLobelia inflata whole — 2 [hp_X]/mLIpecac — 5 [hp_X]/mLGrindelia hirsutula flowering top — 4 [hp_X]/mLEriodictyon californicum leaf — 4 [hp_X]/mLCupric acetate — 6 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BM Private Limited
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2027
Identifiers: Product ID 85816-2013_53e86e30-9938-92d9-e063-6294a90ac1a5SPL ID 53e86e30-9938-92d9-e063-6294a90ac1a5SPL set ID 53e86e23-8619-aef7-e063-6394a90ac38eUNII WQZ3G9PF0H, QR44N9XPJQ, 2166IN72UN, 9PP1T3TC5U, 62I3C8233L, IDB0NAZ6AI, 2Y7TIQ135H, 39M11XPH03

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

N485816201301 followed by a unit qualifier and the quantity

Package 85816-2013-01. 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 10, 2026.

Indications (excerpt from the label)

Indications: For detail please read the enclosed package (Product information leaflet).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)