Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Diathesis V 2 NDC 43857-0638
Ginkgo 6 [hp_X]/mL + 15 more ingredients · Liquid · Oral · BioActive Nutritional, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43857-0638-1 | 43857063801 | 30 mL in 1 BOTTLE, DROPPER (43857-0638-1)Marketed from Feb 13, 2024 |
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 2
- Generic name (nonproprietary)
- ginkgo biloba, pancreas suis, spleen (suis), stomach (suis), germanium sesquioxide, cobaltum metallicum, cysteinum, niccolum metallicum, zincum metallicum, manganese gluconate, alpha-ketoglutaricum acidum, baryta carbonica, fumaricum acidum, natrum oxalaceticum, phosphoricum acidum, phosphorus
- 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]/mLCobalt — 9 [hp_X]/mLCysteine — 9 [hp_X]/mLNickel — 9 [hp_X]/mLZinc — 9 [hp_X]/mLManganese gluconate, Unspecified form — 10 [hp_X]/mLOxogluric acid — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLFumaric acid — 12 [hp_X]/mLSodium diethyl oxalacetate — 12 [hp_X]/mLPhosphoric acid — 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
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)
- Identifiers
- Product ID 43857-0638_807a024f-1eb0-48f1-aed9-dcbde843d8c3SPL ID 807a024f-1eb0-48f1-aed9-dcbde843d8c3SPL set ID 1f389621-b22b-4d6c-9c28-93292eb4eebfUNII 19FUJ2C58T, 9Y3J3362RY, 92AMN5J79Y, T0920P9Z9A, 96WE91N25T, 3G0H8C9362, K848JZ4886, 7OV03QG267, J41CSQ7QDS, 9YY2F980SV, 8ID597Z82X, 6P669D8HQ8, 88XHZ13131, 6CA025Y4FG, E4GA8884NN, 27YLU75U4W
- Pharmacologic class
- Paramagnetic Contrast Agent; Standardized Chemical Allergen
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
N443857063801followed by a unit qualifier and the quantityPackage 43857-0638-01. 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 digestion, dyspepsia, constipation, back pain extending to the legs, headaches extending from ear to ear, burning in stomach, and heartburn from sweets.
Excerpt only. Read the full label for complete information.