United States · FDA National Drug Code directory
Chelidonium comp.
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
- 48951-3281_2df4687c-a157-13ac-e063-6294a90aa494
- Product NDC
- 48951-3281
- Form
- LIQUID
- Composition / generic term
- Chelidonium comp.
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20090901
- Source listing expiry
- 20261231
Source-listed ingredients
- PTERIDIUM AQUILINUM WHOLE — 1 [hp_X]/mL
- TARAXACUM PALUSTRE ROOT — 1 [hp_X]/mL
- URTICA DIOICA — 1 [hp_X]/mL
- CHELIDONIUM MAJUS ROOT — 1 [hp_X]/mL
- MILK THISTLE — 1 [hp_X]/mL
- SALIX PURPUREA BARK — 1 [hp_X]/mL
- ONOPORDUM ACANTHIUM FLOWER — 1 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 60 mL in 1 BOTTLE, DROPPER (48951-3281-3) · 48951-3281-3
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 →