Cardioforce II NDC 43857-0437

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0437Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0437Add 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
43857-0437-1	43857043701	30 mL in 1 BOTTLE, DROPPER (43857-0437-1)Marketed from Mar 2, 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): Cardioforce IISuffix: II
Generic name (nonproprietary): abrotanum, boldo, cimicifuga racemosa, kali phosphoricum, taraxacum officinale, convallaria majalis, magnesia sulphurica, oleander, natrum muriaticum, bellis perennis
Active ingredients: Artemisia abrotanum flowering top — 3 [hp_X]/mLPeumus boldus leaf — 3 [hp_X]/mLBlack cohosh — 3 [hp_X]/mLPotassium phosphate, Dibasic — 3 [hp_X]/mLTaraxacum officinale — 3 [hp_X]/mLConvallaria majalis — 4 [hp_X]/mLMagnesium sulfate heptahydrate — 5 [hp_X]/mLNerium oleander leaf — 8 [hp_X]/mLSodium chloride — 12 [hp_X]/mLBellis perennis whole — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 2, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Increased Large Intestinal Motility (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)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43857-0437_405fc056-72fc-4906-90d3-f5997e893c54SPL ID 405fc056-72fc-4906-90d3-f5997e893c54SPL set ID 733bbb26-7698-4a1b-9dc8-7e3490ffc92bUNII QG07G580U0, Q4EWM09M3O, K73E24S6X9, CI71S98N1Z, 39981FM375, QHH4HVF5QE, SK47B8698T, 7KV510R6H6, 451W47IQ8X, 2HU33I03UYUPC 0210184341787
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N443857043701 followed by a unit qualifier and the quantity

Package 43857-0437-01. 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 17, 2026.

Indications (excerpt from the label)

USES: For temporary relief of mild dizziness, feeling faint; aching of legs, weakness of lower limbs and swelling of legs.** **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)