Cardiotone NDC 43857-0512

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0512Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0512Add 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
43857-0512-1	43857051201	30 mL in 1 BOTTLE, DROPPER (43857-0512-1)Marketed from Apr 2, 2019

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): Cardiotone
Generic name (nonproprietary): adenosinum triphosphoricum dinatrum, cactus grandiflorus, convallaria majalis, heart (suis), magnesium gluconate, potassium gluconate, thyroidinum (suis), ubidecarenonum, germanium sesquioxide, strophanthus hispidus, adonis vernalis, digitalis purpurea
Active ingredients: Adenosine triphosphate disodium — 6 [hp_X]/mLSelenicereus grandiflorus stem — 6 [hp_X]/mLConvallaria majalis — 6 [hp_X]/mLPork heart — 6 [hp_X]/mLMagnesium gluconate — 6 [hp_X]/mLPotassium gluconate — 6 [hp_X]/mLThyroid — 6 [hp_X]/mLUbidecarenone — 6 [hp_X]/mLGermanium sesquioxide — 8 [hp_X]/mLStrophanthus hispidus seed — 10 [hp_X]/mLAdonis vernalis whole — 12 [hp_X]/mLDigitalis — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 2, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43857-0512_26e8971c-369c-45e7-8b2a-c1c5c922b5f4SPL ID 26e8971c-369c-45e7-8b2a-c1c5c922b5f4SPL set ID 282c9ee6-9be6-4ff0-9029-f778d6e9bf55UNII 5L51B4DR1G, 7114SV0MYK, QHH4HVF5QE, X876KJM95L, T42NAD2KHC, 12H3K5QKN9, 6RV024OAUQ, EJ27X76M46, 96WE91N25T, MO892VI77K, DX3ZNI25WK, F1T8QT9U8B
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative; Potassium Salt

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

N443857051201 followed by a unit qualifier and the quantity

Package 43857-0512-01. 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 Aug 28, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of difficulty breathing after walking, tiredness, feeling as if you can't breathe, and profuse perspiration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)