Habifac NDC 59469-141

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-141Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0141Add 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
59469-141-10	59469014110	1 BOTTLE, GLASS in 1 BOX (59469-141-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Apr 12, 2008

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Habifac
Generic name (nonproprietary): formic acid, nitric acid, baptisia tinctoria root, graphite, calcium sulfide, thuja occidentalis leafy twig, cynanchum vincetoxicum leaf, and glechoma hederacea flowering top
Active ingredients: Formic acid — 8 [hp_X]/50mLNitric acid — 6 [hp_X]/50mLBaptisia tinctoria root — 5 [hp_X]/50mLGraphite — 8 [hp_X]/50mLCalcium sulfide — 8 [hp_X]/50mLThuja occidentalis leafy twig — 10 [hp_X]/50mLVincetoxicum hirundinaria leaf — 8 [hp_X]/50mLGlechoma hederacea flowering top — 4 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 12, 2008
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-141_2989c3c6-5187-4615-8c71-31912aa57a10SPL ID 2989c3c6-5187-4615-8c71-31912aa57a10SPL set ID b5fd91ae-3822-421a-a449-4178111950bcUNII 0YIW783RG1, 411VRN1TV4, 5EF0HWI5WU, 4QQN74LH4O, 1MBW07J51Q, 1NT28V9397, 9WLP0FA6U4, 2458J91U39

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

N459469014110 followed by a unit qualifier and the quantity

Package 59469-0141-10. 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 Dec 15, 2022.

Indications (excerpt from the label)

Indications Restorative remedy for minor systemic weakness. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)