Thymoplex NDC 43857-0564

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0564Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0564Add 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
43857-0564-1	43857056401	30 mL in 1 BOTTLE, DROPPER (43857-0564-1)Marketed from Dec 28, 2020

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): Thymoplex
Generic name (nonproprietary): cochlearia armoracia, echinacea (angustifolia), condurango, ginkgo biloba, pinus sylvestris, propolis, spleen (suis), tabebuia impetiginosa, thymus (bovine), bee pollen, hepar sulphuris calcareum, phosphoricum acidum, lachesis mutus
Active ingredients: Horseradish — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLMarsdenia condurango bark — 6 [hp_X]/mLGinkgo — 6 [hp_X]/mLPinus sylvestris leafy twig — 6 [hp_X]/mLPropolis wax — 6 [hp_X]/mLSus scrofa spleen — 6 [hp_X]/mLHandroanthus impetiginosus whole — 6 [hp_X]/mLBos taurus thymus — 6 [hp_X]/mLBee pollen — 8 [hp_X]/mLCalcium sulfide — 8 [hp_X]/mLSus scrofa bone marrow — 8 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLLachesis muta venom — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 28, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 43857-0564_23bcbd5c-d5f0-4516-abdc-cecfb762ec6bSPL ID 23bcbd5c-d5f0-4516-abdc-cecfb762ec6bSPL set ID 1f4a9fda-c53e-4c0c-b624-aa48436c0aeaUNII 8DS6G120HJ, VB06AV5US8, 19FUJ2C58T, Q1RGP4UB73, 6Y8XYV2NOF, 92AMN5J79Y, D65QWF3541, 8XEJ88V2T8, 3729L8MA2C, 1MBW07J51Q, VP2CN2G7Y8, E4GA8884NN, VSW71SS07I
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N443857056401 followed by a unit qualifier and the quantity

Package 43857-0564-01. 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 18, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of sore throat, fever, persistent cough, and fatigue associated with flu.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)