Epiforce E NDC 43857-0570

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0570Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0570Add 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
43857-0570-1	43857057001	30 mL in 1 BOTTLE, DROPPER (43857-0570-1)Marketed from Feb 18, 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): Epiforce E
Generic name (nonproprietary): lappa major, phytolacca decandra, trifolium pratense, hydrocotyle asiatica, arsenicum album, graphites, mezereum
Active ingredients: Arctium lappa root — 3 [hp_X]/mLTrifolium pratense flower — 3 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLCentella asiatica whole — 6 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLGraphite — 12 [hp_X]/mLDaphne mezereum bark — 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: Feb 18, 2021
Listing expires: Dec 31, 2027
Identifiers: Product ID 43857-0570_9c86e023-2d70-4f53-a9f0-fee95bc38971SPL ID 9c86e023-2d70-4f53-a9f0-fee95bc38971SPL set ID ebec32bd-9df0-4a13-b47f-d0caa5f7c9e3UNII 597E9BI3Z3, 4JS0838828, 11E6VI8VEG, 7M867G6T1U, S7V92P67HO, 4QQN74LH4O, X2N6E405GVUPC 0210184340841

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

N443857057001 followed by a unit qualifier and the quantity

Package 43857-0570-01. 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 Mar 5, 2026.

Indications (excerpt from the label)

USES: For temporary relief of skin irritations, urticaria and eczema.** **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)