Thyroid HP NDC 44911-0722

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0722Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0722Add 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
44911-0722-1	44911072201	30 mL in 1 BOTTLE, DROPPER (44911-0722-1)Marketed from Sep 30, 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): Thyroid HP
Generic name (nonproprietary): baryta carbonica, calcarea carbonica, calcarea iodata, fucus vesiculosus, iodium, lapis albus, levothyroxinum, natrum muriaticum, pulsatilla (vulgaris), selenium metallicum, spongia tosta, thyroidinum (suis)
Active ingredients: Barium carbonate — 30 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLCalcium iodide — 30 [hp_X]/mLFucus vesiculosus — 30 [hp_X]/mLIodine — 30 [hp_X]/mLCalcium hexafluorosilicate — 30 [hp_X]/mLLevothyroxine — 30 [hp_X]/mLSodium chloride — 30 [hp_X]/mLPulsatilla vulgaris whole — 30 [hp_X]/mLSelenium — 30 [hp_X]/mLSpongia officinalis skeleton, Roasted — 30 [hp_X]/mLThyroid — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 30, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)Thyroxine (Chemical structure)
Identifiers: Product ID 44911-0722_b7249b51-5056-4cd4-8912-6f51923118e6SPL ID b7249b51-5056-4cd4-8912-6f51923118e6SPL set ID 2f04e425-7160-41a7-aa1e-934db54f1751UNII 6P669D8HQ8, 2E32821G6I, 8EKI9QEE2H, 535G2ABX9M, 9679TC07X4, 2NVP93XVQ3, Q51BO43MG4, 451W47IQ8X, I76KB35JEV, H6241UJ22B, 1PIP394IID, 6RV024OAUQUPC 0363113700961
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder; l-Thyroxine

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

N444911072201 followed by a unit qualifier and the quantity

Package 44911-0722-01. 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 Sep 30, 2024.

Indications (excerpt from the label)

USES: May temporarily relieve: •symptoms due to fatigue after the least exertion •memory issues •constipation** **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)