What is NDC 15631-2638?

15631-2638 is the product NDC for Bryonia Alb, Bryonia alba root 3 [hp_X]/mL liquid, listed with the FDA by Rxhomeo Private Limited d.b.a. Rxhomeo, Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.

Rxhomeo Private Limited d.b.a. Rxhomeo, Inc, NDC labeler code 15631. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Bryonia Alb?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Bryonia Alb NDC 15631-2638 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)15631-2638Labeler and product segments. Claims need a package NDC.

Product NDC at billing width15631-2638Add 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
15631-2638-0	1563126380015631263800	10 mL in 1 BOTTLE (15631-2638-0)Marketed from May 23, 2024
15631-2638-1	1563126380115631263801	30 mL in 1 BOTTLE (15631-2638-1)Marketed from May 23, 2024

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): Bryonia Alb
Generic name (nonproprietary): bryonia alb
Active ingredients: Bryonia alba root — 3 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Rxhomeo Private Limited d.b.a. Rxhomeo, IncNDC labeler code 15631
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 23, 2024
Listing expires: Dec 31, 2026
Identifiers: Product ID 15631-2638_19ba2026-e106-d690-e063-6394a90a5501SPL ID 19ba2026-e106-d690-e063-6394a90a5501SPL set ID 19b9dc92-30be-fd86-e063-6394a90acd7bUNII T7J046YI2B

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

N415631263800 followed by a unit qualifier and the quantity

Package 15631-2638-00. 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 May 31, 2024.

Indications (excerpt from the label)

INDICATIONS Condition listed above or as directed by the physician

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 15631-2638

What is NDC 15631-2638?: 15631-2638 is the product NDC for Bryonia Alb, Bryonia alba root 3 [hp_X]/mL liquid, listed with the FDA by Rxhomeo Private Limited d.b.a. Rxhomeo, Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bryonia Alb.
What is the active ingredient?: Bryonia alba root.
Who is the labeler?: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc, NDC labeler code 15631. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bryonia Alb?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.