Diathesis I NDC 43857-0249

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0249Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0249Add 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
43857-0249-1	43857024901	30 mL in 1 BOTTLE, DROPPER (43857-0249-1)Marketed from Jan 9, 2014

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 ISuffix: I
Generic name (nonproprietary): manganum metallicum, germanium sesquioxide, fel tauri, hepar suis, ginkgo biloba, cysteinum, manganese gluconate, alpha-ketoglutaricum acidum, arsenicum album, fumaricum acidum, phosphorus, sodium oxalate, sulphur
Active ingredients: Manganese — 9 [hp_X]/mLGermanium sesquioxide — 8 [hp_X]/mLBos taurus bile — 6 [hp_X]/mLPork liver — 6 [hp_X]/mLGinkgo — 6 [hp_X]/mLCysteine — 9 [hp_X]/mLManganese gluconate — 10 [hp_X]/mL.alpha.-ketoglutaric acid — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLFumaric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLSodium oxalate — 12 [hp_X]/mLSulfur — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritionals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 9, 2014
Listing expires: Dec 31, 2026
Other FDA classes: Magnetic Resonance Contrast Activity (Mechanism)
Identifiers: Product ID 43857-0249_8abac30f-8abf-4d91-88b6-f4361ca97586SPL ID 8abac30f-8abf-4d91-88b6-f4361ca97586SPL set ID e8c3b763-7d54-48b1-8db8-a5b47ce7aeebUNII 42Z2K6ZL8P, 96WE91N25T, ET3651ZLOU, 6EC706HI7F, 19FUJ2C58T, K848JZ4886, 9YY2F980SV, 8ID597Z82X, S7V92P67HO, 88XHZ13131, 27YLU75U4W, 7U0V68LT9X, 70FD1KFU70
Pharmacologic class: 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

N443857024901 followed by a unit qualifier and the quantity

Package 43857-0249-01. 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 Jul 13, 2018.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of inflammation of bones or joints, with nightly digging pains, general soreness and aching soreness over entire body when touched, and burning in soles and hands at night.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)