Diathesis II NDC 43857-0372

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0372Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0372Add 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
43857-0372-1	43857037201	30 mL in 1 BOTTLE, DROPPER (43857-0372-1)Marketed from Jul 9, 2015

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 IISuffix: II
Generic name (nonproprietary): germanium sesquioxide, cuprum metallicum, manganum metallicum, intestine (suis), lung (suis), cysteinum, manganese gluconate, alpha-ketoglutaricum acidum, arsenicum album, calcarea carbonica, fumaricum acidum, natrum oxalaceticum, phosphorus
Active ingredients: Germanium sesquioxide — 8 [hp_X]/mLCopper — 8 [hp_X]/mLManganese — 8 [hp_X]/mLPork intestine — 8 [hp_X]/mLSus scrofa lung — 8 [hp_X]/mLCysteine — 9 [hp_X]/mLManganese gluconate — 10 [hp_X]/mLOxogluric acid — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLFumaric acid — 12 [hp_X]/mLSodium diethyl oxalacetate — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 9, 2015
Listing expires: Dec 31, 2026
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 43857-0372_e9e9be76-4b66-42b5-80de-bea58b041b1bSPL ID e9e9be76-4b66-42b5-80de-bea58b041b1bSPL set ID 240a5573-0603-4201-ab11-39b894b8794eUNII 96WE91N25T, 789U1901C5, 42Z2K6ZL8P, 40GMI0R60L, 7GL3G1COB3, K848JZ4886, 9YY2F980SV, 8ID597Z82X, S7V92P67HO, 2E32821G6I, 88XHZ13131, 6CA025Y4FG, 27YLU75U4W
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

N443857037201 followed by a unit qualifier and the quantity

Package 43857-0372-01. 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 27, 2017.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of inflammation of bones or joints, with nightly digging pains, general soreness & aching, spasmodic states such as intestinal colic, cramps of calf muscles, & spasmodic coughing.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)