Arterioforce II NDC 43857-0568

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0568Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0568Add 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
43857-0568-1	43857056801	30 mL in 1 BOTTLE, DROPPER (43857-0568-1)Marketed from Apr 19, 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): Arterioforce IISuffix: II
Generic name (nonproprietary): baptisia tinctoria, echinacea (angustifolia), myrrha, nasturtium aquaticum, phytolacca decandra, trigonella foenum-graecum, hydrastis canadensis, kali iodatum, arnica montana, cactus grandiflorus, propolis, baryta carbonica, conium maculatum, secale cornutum
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLMyrrh — 4 [hp_X]/mLNasturtium officinale — 4 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLFenugreek seed — 4 [hp_X]/mLGoldenseal — 5 [hp_X]/mLPotassium iodide — 5 [hp_X]/mLArnica montana whole — 6 [hp_X]/mLSelenicereus grandiflorus stem — 6 [hp_X]/mLPropolis wax — 6 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLClaviceps purpurea sclerotium — 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 19, 2021
Listing expires: Dec 31, 2027
Identifiers: Product ID 43857-0568_40bd7778-8dfe-4847-9678-757f2b141c83SPL ID 40bd7778-8dfe-4847-9678-757f2b141c83SPL set ID ef98fbda-6815-4d0d-b07e-62ce420c4deeUNII 5EF0HWI5WU, VB06AV5US8, JC71GJ1F3L, YH89GMV676, 11E6VI8VEG, 654825W09Z, ZW3Z11D0JV, 1C4QK22F9J, O80TY208ZW, 7114SV0MYK, 6Y8XYV2NOF, 6P669D8HQ8, Q28R5GF371, 01G9XEA93NUPC 0210184340674

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

N443857056801 followed by a unit qualifier and the quantity

Package 43857-0568-01. 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 11, 2026.

Indications (excerpt from the label)

USES: For temporary relief of swollen extremities that feel bruised & sore, cold, clammy feet, mild burning pains in lower limbs, leg cramps.** **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)