United States · FDA National Drug Code directory

DEFAETON

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 59469-133_eac362c3-95fe-4916-b408-014484204823
Product NDC: 59469-133
Form: SOLUTION/ DROPS
Composition / generic term: Peumus boldus Leaf, Dioscorea villosa Tuber, Strychnos ignatii Seed, Cynara scolymus Whole, Fumaria officinalis Whole, Frangula Alnus Bark, and Rheum officinale Root
Labeler: PEKANA Naturheilmittel GmbH
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 20081211
Source listing expiry: 20261231

Source-listed ingredients

PEUMUS BOLDUS LEAF — 6 [hp_X]/50mL
DIOSCOREA VILLOSA TUBER — 4 [hp_X]/50mL
STRYCHNOS IGNATII SEED — 6 [hp_X]/50mL
CYNARA SCOLYMUS WHOLE — 12 [hp_X]/50mL
FUMARIA OFFICINALIS WHOLE — 6 [hp_X]/50mL
FRANGULA ALNUS BARK — 8 [hp_X]/50mL
RHEUM OFFICINALE ROOT — 8 [hp_X]/50mL

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE, GLASS in 1 BOX (59469-133-10) / 50 mL in 1 BOTTLE, GLASS · 59469-133-10
1 BOTTLE, GLASS in 1 BOX (59469-133-40) / 100 mL in 1 BOTTLE, GLASS · 59469-133-40

Source and coverage

Open FDA National Drug Code directory →

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →