Ginkgo Tonic NDC 43857-0383

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0383Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0383Add 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
43857-0383-1	43857038301	60 mL in 1 BOTTLE, DROPPER (43857-0383-1)Marketed from Nov 30, 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): Ginkgo Tonic
Generic name (nonproprietary): aralia quinquefolia, ginkgo biloba, hydrocotyle asiatica, polygonum multiflorum, aronia melanocarpa, vaccinium myrtillus, germanium sesquioxide, aurum metallicum, baryta muriatica, kali phosphoricum, plumbum metallicum, secale cornutum, tabacum, viscum album, ubidecarenonum, adenosinum triphosphoricum dinatrum
Active ingredients: American ginseng — 1 [hp_X]/mLGinkgo — 1 [hp_X]/mLCentella asiatica whole — 1 [hp_X]/mLFallopia multiflora root — 1 [hp_X]/mLAronia melanocarpa fruit — 3 [hp_X]/mLBilberry — 3 [hp_X]/mLGermanium sesquioxide — 8 [hp_X]/mLGold — 12 [hp_X]/mLBarium chloride dihydrate — 12 [hp_X]/mLPotassium phosphate, Dibasic — 12 [hp_X]/mLLead — 12 [hp_X]/mLClaviceps purpurea sclerotium — 12 [hp_X]/mLTobacco leaf — 12 [hp_X]/mLViscum album fruiting top — 12 [hp_X]/mLUbidecarenone — 12 [hp_X]/mLAdenosine triphosphate disodium — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 30, 2015
Listing expires: Dec 31, 2026
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)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 43857-0383_2290ed30-0d34-4259-a7b0-0ee1a97a691aSPL ID 2290ed30-0d34-4259-a7b0-0ee1a97a691aSPL set ID f26ecaab-d3fc-47de-a0ef-b0a3f0f4f71fUNII 8W75VCV53Q, 19FUJ2C58T, 7M867G6T1U, AUZ3VD75MC, S935718Z2Q, 9P2U39H18W, 96WE91N25T, 79Y1949PYO, EL5GJ3U77E, CI71S98N1Z, 2P299V784P, 01G9XEA93N, 6YR2608RSU, BK9092J5MP, EJ27X76M46, 5L51B4DR1G
Pharmacologic class: Non-Standardized Plant Allergenic Extract; 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

N443857038301 followed by a unit qualifier and the quantity

Package 43857-0383-01. 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 Oct 17, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of coldness of the extremities; fingers and feet bluish and numb; shortness of breath on least exertion; fatigue; exhaustion and poor memory.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)