Senility HP NDC 43857-0254

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0254Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0254Add 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
43857-0254-1	43857025401	30 mL in 1 BOTTLE, DROPPER (43857-0254-1)Marketed from Feb 23, 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): Senility HP
Generic name (nonproprietary): anacardium orientale, belladonna, hyoscyamus niger, veratrum album, baryta carbonica, lachesis mutus, phosphorus, stramonium
Active ingredients: Semecarpus anacardium juice — 30 [hp_X]/mLAtropa belladonna — 30 [hp_X]/mLHyoscyamus niger — 30 [hp_X]/mLVeratrum album root — 30 [hp_X]/mLBarium carbonate — 30 [hp_C]/mLLachesis muta venom — 30 [hp_C]/mLPhosphorus — 30 [hp_C]/mLDatura stramonium — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 13, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 43857-0254_fb3f2ef5-8647-4b6c-83aa-146f94d1754aSPL ID fb3f2ef5-8647-4b6c-83aa-146f94d1754aSPL set ID 214cf942-5277-4f4b-af7d-a9fcc6c8bd37UNII Y0F0BU8RDU, WQZ3G9PF0H, 4WRK2153H3, QNS6W5US1Z, 6P669D8HQ8, VSW71SS07I, 27YLU75U4W, G6W4F0V8Z3

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

N443857025401 followed by a unit qualifier and the quantity

Package 43857-0254-01. 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 Feb 23, 2017.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of symptoms due to Alzheimer's disease.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)