Scrophulous HP NDC 44911-0404

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0404Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0404Add 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
44911-0404-1	44911040401	30 mL in 1 BOTTLE, DROPPER (44911-0404-1)Marketed from Nov 15, 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, gnaphalium polycephalum, 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]/mLPseudognaphalium obtusifolium — 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: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 15, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0404_d90bfbfa-2017-4c56-986a-5ffa4d5ec178SPL ID d90bfbfa-2017-4c56-986a-5ffa4d5ec178SPL set ID e50eb26b-6843-4b8f-8ea5-3d5f57a3e7b4UNII 6P669D8HQ8, SBV4XY874G, 2E32821G6I, F5452U54PN, 36XQ854NWW, 324Y4038G2, 11E6VI8VEG, 6IO182RP7A, ETJ7Z6XBU4UPC 0363113701647

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

N444911040401 followed by a unit qualifier and the quantity

Package 44911-0404-01. 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 30, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms due to lymphatic issues, such as glandular swelling, fluid retention, and being easily susceptible to infections.** **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)