Epiforce P-HP NDC 43857-0604

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0604Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0604Add 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
43857-0604-1	43857060401	30 mL in 1 BOTTLE, DROPPER (43857-0604-1)Marketed from Jun 15, 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 P-HP
Generic name (nonproprietary): arsenicum album, borax, graphites, natrum muriaticum, sepia, sulphur
Active ingredients: Arsenic trioxide — 30 [hp_X]/mLSodium borate — 30 [hp_X]/mLGraphite — 30 [hp_X]/mLSodium chloride — 30 [hp_X]/mLSepia officinalis juice — 30 [hp_X]/mLSulfur — 30 [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 15, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 43857-0604_6524482b-75e7-4ff4-a534-f7ab7e69595eSPL ID 6524482b-75e7-4ff4-a534-f7ab7e69595eSPL set ID 250441d1-e261-417e-9100-700368ea38fdUNII S7V92P67HO, 91MBZ8H3QO, 4QQN74LH4O, 451W47IQ8X, QDL83WN8C2, 70FD1KFU70

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

N443857060401 followed by a unit qualifier and the quantity

Package 43857-0604-01. 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 Sep 11, 2023.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of symptoms due to skin eruptions.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)