Cardiacforce NDC 43857-0607

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0607Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0607Add 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
43857-0607-1	43857060701	30 mL in 1 BOTTLE, DROPPER (43857-0607-1)Marketed from Jun 21, 2021

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): Cardiacforce
Generic name (nonproprietary): juglans nigra, leonurus cardiaca, convallaria majalis, magnesia sulphurica, iberis amara, kali chloricum, adonis vernalis, digitalis purpurea, lycopus virginicus, phosphorus
Active ingredients: Black walnut — 3 [hp_X]/mLLeonurus cardiaca whole — 3 [hp_X]/mLConvallaria majalis — 4 [hp_X]/mLMagnesium sulfate heptahydrate — 4 [hp_X]/mLIberis amara seed — 6 [hp_X]/mLPotassium chlorate — 6 [hp_X]/mLAdonis vernalis whole — 10 [hp_X]/mLDigitalis — 12 [hp_X]/mLLycopus virginicus whole — 12 [hp_X]/mLPhosphorus — 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: Jun 21, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)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)Nut Proteins (EXT)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43857-0607_21c6cee6-6f78-4c0b-a4e7-bdcb7854fb9dSPL ID 21c6cee6-6f78-4c0b-a4e7-bdcb7854fb9dSPL set ID 9bdb3774-6ee5-4622-8fe3-5bd5f0e2ab56UNII 02WM57RXZJ, 8NC0C2YXK0, QHH4HVF5QE, SK47B8698T, T90A7M66YF, H35KS68EE7, DX3ZNI25WK, F1T8QT9U8B, TWH5125Q6F, 27YLU75U4W
Pharmacologic class: Calculi Dissolution Agent; Non-Standardized Food Allergenic Extract; 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

N443857060701 followed by a unit qualifier and the quantity

Package 43857-0607-01. 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 Apr 3, 2026.

Indications (excerpt from the label)

USES: For temporary relief of lightheadedness & nervous anxiety, dizziness on rising or lying down, sensation as if heart stops & then starts again.** **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)