Cardio Tonic NDC 44911-0409

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0409Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0409Add 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
44911-0409-1	44911040901	30 mL in 1 BOTTLE, DROPPER (44911-0409-1)Marketed from Jan 3, 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): Cardio Tonic
Generic name (nonproprietary): cactus grandiflorus, l-carnitine, linum usitatissimum, strophanthus hispidus, borago officinalis, heart (suis), kali carbonicum, kali nitricum, thyroidinum (suis), adonis vernalis, digitalis purpurea, lycopus virginicus
Active ingredients: Selenicereus grandiflorus stem — 3 [hp_X]/mLLevocarnitine — 3 [hp_X]/mLFlax seed — 4 [hp_X]/mLStrophanthus hispidus seed — 4 [hp_X]/mLBorage — 6 [hp_X]/mLPork heart — 6 [hp_X]/mLPotassium carbonate — 6 [hp_X]/mLPotassium nitrate — 6 [hp_X]/mLThyroid — 6 [hp_X]/mLAdonis vernalis whole — 12 [hp_X]/mLDigitalis — 12 [hp_X]/mLLycopus virginicus whole — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 3, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Carnitine (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 44911-0409_dab19f2d-4f7a-4608-9570-33fca0c25b49SPL ID dab19f2d-4f7a-4608-9570-33fca0c25b49SPL set ID 3b69f1ff-ecfc-48ca-86d8-7130f32cb772UNII 7114SV0MYK, 0G389FZZ9M, 4110YT348C, MO892VI77K, PB618V0K2W, X876KJM95L, BQN1B9B9HA, RU45X2JN0Z, 6RV024OAUQ, DX3ZNI25WK, F1T8QT9U8B, TWH5125Q6FUPC 0363113701302
Pharmacologic class: Carnitine Analog; 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

N444911040901 followed by a unit qualifier and the quantity

Package 44911-0409-01. 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 24, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve nervous anxiety with tiredness, difficulty breathing at night while sleeping, coldness of hands and feet, and swelling of the extremities.** **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)