Anx HP NDC 43857-0041

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0041Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0041Add 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
43857-0041-1	43857004101	30 mL in 1 BOTTLE, DROPPER (43857-0041-1)Marketed from Jun 14, 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): Anx HP
Generic name (nonproprietary): arsenicum album, calcarea carbonica, ignatia amara, kali carbonicum, lachesis mutus, natrum muriaticum
Active ingredients: Arsenic trioxide — 30 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLStrychnos ignatii seed — 30 [hp_X]/mLPotassium carbonate — 30 [hp_X]/mLLachesis muta venom — 30 [hp_X]/mLSodium chloride — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLPulsatilla vulgaris — 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: Jan 24, 2013
Listing expires: Dec 31, 2027
Identifiers: Product ID 43857-0041_ee809460-8cd6-4746-8526-8d88fcd5247aSPL ID ee809460-8cd6-4746-8526-8d88fcd5247aSPL set ID 96035891-aea3-4138-bb26-801ad819f639UNII S7V92P67HO, 2E32821G6I, 1NM3M2487K, BQN1B9B9HA, VSW71SS07I, 451W47IQ8X, 27YLU75U4W, I76KB35JEVUPC 0210184341428

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

N443857004101 followed by a unit qualifier and the quantity

Package 43857-0041-01. 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 30, 2026.

Indications (excerpt from the label)

USES: For temporary relief of symptoms due to anxiety.** **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)