NDC codes

FDA NDC Directory
Product NDC (as listed)43857-0172Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43857-0172Add 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
43857-0172-14385701720130 mL in 1 BOTTLE, DROPPER (43857-0172-1)Marketed from Nov 3, 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)
Diathesis V 1Suffix: V 1
Generic name (nonproprietary)
ginkgo biloba, pancreas (suis), spleen (suis), stomach (suis), germanium sesquioxide, cuprum metallicum, cysteinum, zincum metallicum, manganese gluconate, alpha-ketoglutaricum acidum, fumaricum acidum, natrum oxalaceticum
Active ingredients
Ginkgo — 6 [hp_X]/mLSus scrofa pancreas — 6 [hp_X]/mLSus scrofa spleen — 6 [hp_X]/mLSus scrofa stomach — 6 [hp_X]/mLGermanium sesquioxide — 8 [hp_X]/mLCopper — 9 [hp_X]/mLCysteine — 9 [hp_X]/mLZinc — 9 [hp_X]/mLManganese gluconate — 10 [hp_X]/mL.alpha.-ketoglutaric acid — 12 [hp_X]/mLFumaric acid — 12 [hp_X]/mLSodium diethyl oxalacetate — 12 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)
Identifiers
Product ID 43857-0172_a38f0abb-4b64-4120-bd4f-08cae1f2ec47SPL ID a38f0abb-4b64-4120-bd4f-08cae1f2ec47SPL set ID 58a16fcf-b05f-41a9-a580-41da6300ac7fUNII 19FUJ2C58T, 9Y3J3362RY, 92AMN5J79Y, T0920P9Z9A, 96WE91N25T, 789U1901C5, K848JZ4886, J41CSQ7QDS, 9YY2F980SV, 8ID597Z82X, 88XHZ13131, 6CA025Y4FG
Pharmacologic class
Copper-containing Intrauterine Device; Paramagnetic Contrast Agent

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

N443857017201 followed by a unit qualifier and the quantity

Package 43857-0172-01. 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 weak memory, sensitivity to noises, left ovarian pain, restlessness, depressed feelings, cramps of calf muscles, colic & spasmodic coughing.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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