FDA.reportPublic FDA data

Chelidonium Curcuma P

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-04-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:09:23

Label at a glance#

ProductChelidonium Curcuma P
Active ingredientCHELIDONIUM MAJUS ROOT, TURMERIC
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: 25gm Chelidonium (Greater celandine) 1X, 25gm Curcuma (Turmeric) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Propolis

OTC - PURPOSE SECTION

Use: Temporary relief of digestive upset.

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.

REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 30 DAYS OF OPENING.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ChelidoniumCurcumaPLiquidChelidoniumCurcumaPLiquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3154-3Chelidonium Curcuma P60 mL in 1 BOTTLE, DROPPERLIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3154CHELIDONIUM CURCUMA P LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20180425_59566c5e-02bf-42a6-8a63-53d5bfe30909.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CHELIDONIUM MAJUS ROOTACTIVE INGREDIENTFLT36UCF0N1
TURMERICACTIVE INGREDIENT856YO1Z64F1
CHELIDONIUM MAJUS ROOTACTIVE MOIETYFLT36UCF0N1
TURMERICACTIVE MOIETY856YO1Z64F1
PROPOLIS WAXINACTIVE INGREDIENT6Y8XYV2NOF1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-315448951-3154-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPOLIS WAX6Y8XYV2NOFIACT
CHELIDONIUM MAJUS ROOTFLT36UCF0NACTIB
TURMERIC856YO1Z64FACTIB

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
6a9df35e-68f2-6759-e053-2a91aa0afc2a59566c5e-02bf-42a6-8a63-53d5bfe309092018-04-24WarningsExact identifier
spl id: 6a9df35e-68f2-6759-e053-2a91aa0afc2a
spl set id: 59566c5e-02bf-42a6-8a63-53d5bfe30909

Reported adverse events (FAERS/openFDA)#

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