Thyroid-Adrenal NDC 55714-2564

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-2564Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-2564Add 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
55714-2564-1	55714256401	30 mL in 1 BOTTLE, GLASS (55714-2564-1)Marketed from Oct 30, 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): Thyroid-Adrenal
Generic name (nonproprietary): adrenalinum, thyroidinum, aloe, calc. carb., chelidonium majus, conium, graphites, iodium, lachesis, lycopodium, lycopus virginicus, phytolacca, rhus toxicodendron, silicea, spongia, echinacea
Active ingredients: Epinephrine — 15 [hp_X]/mLThyroid, Unspecified — 15 [hp_X]/mLAloe — 15 [hp_X]/mLOyster shell calcium carbonate, Crude — 15 [hp_X]/mLChelidonium majus — 15 [hp_X]/mLConium maculatum flowering top — 15 [hp_X]/mLGraphite — 15 [hp_X]/mLIodine — 15 [hp_X]/mLLachesis muta venom — 15 [hp_X]/mLLycopodium clavatum spore — 15 [hp_X]/mLLycopus virginicus — 15 [hp_X]/mLPhytolacca americana root — 15 [hp_X]/mLToxicodendron pubescens leaf — 15 [hp_X]/mLSilicon dioxide — 15 [hp_X]/mLSpongia officinalis skeleton, Roasted — 15 [hp_X]/mLEchinacea, Unspecified — 6 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 30, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Catecholamines (Chemical structure)
Identifiers: Product ID 55714-2564_b5971c5b-0539-0e97-e053-2a95a90a8121SPL ID b5971c5b-0539-0e97-e053-2a95a90a8121SPL set ID b59731a2-c775-7e8a-e053-2a95a90a9062UNII YKH834O4BH, 0B4FDL9I6P, V5VD430YW9, 2E32821G6I, 7E889U5RNN, Q28R5GF371, 4QQN74LH4O, 9679TC07X4, VSW71SS07I, C88X29Y479, TWH5125Q6F, 11E6VI8VEG, 6IO182RP7A, ETJ7Z6XBU4, 1PIP394IID, 4N9P6CC1DX
Pharmacologic class: Catecholamine; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N455714256401 followed by a unit qualifier and the quantity

Package 55714-2564-01. 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 Dec 3, 2020.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for associated symptoms such as rapid or sluggish metabolism, weight fluctuation, fatigue and hair loss.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)