Defaeton NDC 59469-133

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-133Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0133Add 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
59469-133-10	59469013310	1 BOTTLE, GLASS in 1 BOX (59469-133-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Dec 11, 2008
59469-133-40	59469013340	1 BOTTLE, GLASS in 1 BOX (59469-133-40) / 100 mL in 1 BOTTLE, GLASSMarketed from May 1, 2017

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): Defaeton
Generic name (nonproprietary): peumus boldus leaf, dioscorea villosa tuber, strychnos ignatii seed, cynara scolymus whole, fumaria officinalis whole, frangula alnus bark, and rheum officinale root
Active ingredients: Peumus boldus leaf — 6 [hp_X]/50mLDioscorea villosa tuber — 4 [hp_X]/50mLStrychnos ignatii seed — 6 [hp_X]/50mLCynara scolymus whole — 12 [hp_X]/50mLFumaria officinalis whole — 6 [hp_X]/50mLFrangula alnus bark — 8 [hp_X]/50mLRheum officinale root — 8 [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: Dec 11, 2008
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-133_eac362c3-95fe-4916-b408-014484204823SPL ID eac362c3-95fe-4916-b408-014484204823SPL set ID 7099c648-4de6-4600-9fbc-f9bc600dcf7aUNII Q4EWM09M3O, IWY3IWX2G8, 1NM3M2487K, 9N3437ZUU0, DM87NN227Z, S2D77IH61R, A47JP5ZG9M

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

N459469013310 followed by a unit qualifier and the quantity

Package 59469-0133-10. 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 Jan 11, 2023.

Indications (excerpt from the label)

Indications For relief of occasional constipation. 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)