Bio Viscum Phase NDC 43742-1262

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1262Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1262Add 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
43742-1262-1	43742126201	30 mL in 1 BOTTLE, DROPPER (43742-1262-1)Marketed from Jul 20, 2018

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): Bio Viscum Phase
Generic name (nonproprietary): viscum album, l-tryptophan, adenosinum cyclophosphoricum, serotonin (hydrochloride), mercurius iodatus flavus
Active ingredients: Viscum album fruiting top — 3 [hp_X]/mLSerotonin hydrochloride — 6 [hp_X]/mLTryptophan — 8 [hp_X]/mLAdenosine cyclic phosphate — 8 [hp_X]/mLMercurous iodide — 10 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 20, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-1262_e8d06e55-c2d5-438d-8365-dc9c058377b9SPL ID e8d06e55-c2d5-438d-8365-dc9c058377b9SPL set ID d415ff1e-c5f7-43a5-afd5-58b24db86bebUNII BK9092J5MP, GKN429M9VS, 8DUH1N11BX, E0399OZS9N, HT0935F2JRUPC 0810151881744

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

N443742126201 followed by a unit qualifier and the quantity

Package 43742-1262-01. 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 Oct 23, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • frontal headaches • joint pain • aching pain • stabbing nerve pain These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)