Thymupar NDC 44911-0427

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0427Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0427Add 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
44911-0427-1	44911042701	30 mL in 1 BOTTLE, DROPPER (44911-0427-1)Marketed from Jun 6, 2017

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): Thymupar
Generic name (nonproprietary): baptisia tinctoria, echinacea (angustifolia), hydrastis canadensis, thymus (suis), arsenicum album, belladonna, hepar sulphuris calcareum, iridium metallicum, lachesis mutus
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLGoldenseal — 6 [hp_X]/mLSus scrofa thymus — 6 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLAtropa belladonna whole — 12 [hp_X]/mLCalcium sulfide — 12 [hp_X]/mLIridium — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 6, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0427_be4cee64-ec11-4d67-bd94-4da860fd2747SPL ID be4cee64-ec11-4d67-bd94-4da860fd2747SPL set ID 4535ac9d-f58a-47e8-afba-e35df4806dd3UNII 5EF0HWI5WU, VB06AV5US8, ZW3Z11D0JV, 7B69B0BD62, S7V92P67HO, DSV74G1P2J, 1MBW07J51Q, 44448S9773, VSW71SS07I

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

N444911042701 followed by a unit qualifier and the quantity

Package 44911-0427-01. 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 30, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of irritated throat, fever, persistent cough, fatigue associated with flu. ** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)