FDA.reportPublic FDA data

PTERIDIUM AQUILINUM WHOLE

Manufacturer
Uriel Pharmacy, Inc
Effective date
2025-02-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:32:07

Label at a glance#

ProductChelidonium comp.
Active ingredientPTERIDIUM AQUILINUM WHOLE, TARAXACUM PALUSTRE ROOT, URTICA DIOICA, CHELIDONIUM MAJUS ROOT, MILK THISTLE, SALIX PURPUREA BARK, ONOPORDUM ACANTHIUM FLOWER
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 100gm contains: 16.7gm Carduus marianus e sem (Milk thistle) 1X, 5.04gm Chelidonium e rad. (Greater Celandine) 1X, 5.55gm Onopordon (Cotton thistle) 1X, 16.7gm Pteridium aquilinum e fol. (Eagle fern) 1X, 16.7gm Salix purpurea e fol. (Purple willow) 1X, 3.33gm Taraxacum e pl. tota (Dandelion) 1X, 3.33gm Urtica diocia e pl. tota (Stinging nettle) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 30% Organic cane alcohol

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Supports normal liver function.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Chelidonium comp. LiquidChelidonium comp. Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3281-3Chelidonium comp.60 mL in 1 BOTTLE, DROPPERLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3281CHELIDONIUM COMP. LIQUID [URIEL PHARMACY, INC]1Current NDC, 1 package rows20250214_2df4687c-a156-13ac-e063-6294a90aa494.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-328148951-3281-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
PTERIDIUM AQUILINUM WHOLE05T3M06HCMACTIB
TARAXACUM PALUSTRE ROOTGCZ4W7077CACTIB
URTICA DIOICA710FLW4U46ACTIB
WATER059QF0KO0RIACT
CHELIDONIUM MAJUS ROOTFLT36UCF0NACTIB
MILK THISTLEU946SH95EEACTIB
SALIX PURPUREA BARK287VJO13M9ACTIB
ALCOHOL3K9958V90MIACT
ONOPORDUM ACANTHIUM FLOWERAP97AUF88EACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Chelidonium comp.CHELIDONIUM COMP.Uriel Pharmacy, Inc2df4687c-a156-13ac-e063-6294a90aa4942025-02-12WarningsExact identifier
ndc (package): 48951-3281-3
ndc (product): 48951-3281
ndc11 (package): 48951328103
spl id: 2df4687c-a157-13ac-e063-6294a90aa494
spl set id: 2df4687c-a156-13ac-e063-6294a90aa494

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.