Venoforce II NDC 43857-0519

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0519Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0519Add 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
43857-0519-1	43857051901	30 mL in 1 BOTTLE, DROPPER (43857-0519-1)Marketed from Dec 19, 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): Venoforce IISuffix: II
Generic name (nonproprietary): collinsonia canadensis, hamamelis virginiana, aesculus hippocastanum, belladonna, calcarea fluorica, carduus marianus, pulsatilla (pratensis), secale cornutum, vipera berus
Active ingredients: Collinsonia canadensis root — 3 [hp_X]/mLHamamelis virginiana root bark/stem bark — 3 [hp_X]/mLHorse chestnut — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLCalcium fluoride — 12 [hp_X]/mLMilk thistle — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLClaviceps purpurea sclerotium — 12 [hp_X]/mLVipera berus venom — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Prescription drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 19, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 43857-0519_acd1dbe0-c798-4873-b89c-8265749b3ca6SPL ID acd1dbe0-c798-4873-b89c-8265749b3ca6SPL set ID a5226861-ad3e-4352-b31c-612f7fa993ddUNII O2630F3XDR, T7S323PKJS, 3C18L6RJAZ, WQZ3G9PF0H, O3B55K4YKI, U946SH95EE, 8E272251DI, 01G9XEA93N, 0ORO6NCA4M

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

N443857051901 followed by a unit qualifier and the quantity

Package 43857-0519-01. 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 18, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of achiness and minor swelling of the lower extremities, aching and soreness in limbs and tired feeling in legs and tenderness, and achiness from distended veins.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)