Scrophulous HP NDC 43857-0267

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0267Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0267Add 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
43857-0267-1	43857026701	30 mL in 1 BOTTLE, DROPPER (43857-0267-1)Marketed from Apr 14, 2016

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): Scrophulous HPSuffix: HP
Generic name (nonproprietary): baryta carbonica, bromium, calcarea carbonica, ferrum iodatum, mercurius solubilis, phytolacca decandra, rhus tox, silicea
Active ingredients: Barium carbonate — 30 [hp_X]/mLBromine — 30 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLFerrous iodide — 30 [hp_X]/mLMercurius solubilis — 30 [hp_X]/mLPhytolacca americana root — 30 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mLSilicon dioxide — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 1, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 43857-0267_f6c9d1f8-892d-4811-ac57-e8fcdc86c8f0SPL ID f6c9d1f8-892d-4811-ac57-e8fcdc86c8f0SPL set ID 3421f76b-bcde-42b5-a04b-05099520e661UNII 6P669D8HQ8, SBV4XY874G, 2E32821G6I, F5452U54PN, 324Y4038G2, 11E6VI8VEG, 6IO182RP7A, ETJ7Z6XBU4UPC 0210184340728

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

N443857026701 followed by a unit qualifier and the quantity

Package 43857-0267-01. 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 Dec 18, 2025.

Indications (excerpt from the label)

USES: For temporary relief of symptoms due to glandular swelling and lymphatic affliction.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)