NDC codes

FDA NDC Directory
Product NDC (as listed)43857-0540Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43857-0540Add 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 NDC11-digit (billing)PackageCopy
43857-0540-14385705400130 mL in 1 BOTTLE, DROPPER (43857-0540-1)Marketed from Oct 24, 2019

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)
Radiation
Generic name (nonproprietary)
capsicum annuum, cetraria islandica, fucus vesiculosus, glandula suprarenalis suis, thyroidinum (suis), cadmium iodatum, hydrangea arborescens, phosphoricum acidum, phosphorus, pulsatilla (pratensis), strontium carbonicum, uranium nitricum, x-ray
Active ingredients
Capsicum — 3 [hp_X]/mLCetraria islandica whole — 3 [hp_X]/mLFucus vesiculosus — 3 [hp_X]/mLSus scrofa adrenal gland — 8 [hp_X]/mLThyroid — 8 [hp_X]/mLCadmium iodide — 12 [hp_X]/mLHydrangea arborescens root — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLStrontium carbonate — 12 [hp_X]/mLUranyl nitrate hexahydrate — 30 [hp_X]/mLAlcohol, X-ray exposed (1000 rad) — 30 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Marketing end
Other FDA classes
Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers
Product ID 43857-0540_b7adf3e4-9cc6-4db4-9e8e-83a068f9cdf3SPL ID b7adf3e4-9cc6-4db4-9e8e-83a068f9cdf3SPL set ID 1c49738c-6750-47de-a623-96f53eab7badUNII 00UK7646FG, BJ7YPN79A1, 535G2ABX9M, 398IYQ16YV, 6RV024OAUQ, 2F2UPU4KCW, SFK828Q2DE, E4GA8884NN, 27YLU75U4W, 8E272251DI, 41YPU4MMCA, 3V057702FY, 6PRJ93602P
Pharmacologic class
Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N443857054001 followed by a unit qualifier and the quantity

Package 43857-0540-01. 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 .

Indications (excerpt from the label)

INDICATIONS: For temporary relief of cough with expectoration, skin cracked with eruptions and weakness and trembling of arms and hands with numbness.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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