FDA.reportPublic FDA data

Cordia

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-04-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:59:32

Label at a glance#

ProductCordia
Active ingredientACONITUM NAPELLUS, ARNICA MONTANA FLOWER, GOLD, SELENICEREUS GRANDIFLORUS STEM, CONVALLARIA MAJALIS, HAWTHORN LEAF WITH FLOWER, SAFFRON, DIGITALIS, EQUISETUM ARVENSE TOP, ST. JOHN'S WORT, LEONURUS CARDIACA FLOWERING TOP, MELISSA OFFICINALIS, SEDUM ROSEUM WHOLE, ROSMARINUS OFFICINALIS FLOWERING TOP, RUTA GRAVEOLENS FLOWERING TOP, SANGUINARIA CANADENSIS ROOT
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: Aconitum (Monkshood) 6X, Arnica 6X, Aurum colloidale (Colloidal gold) 6X, Cactus (Queen of the night) 6X, Convallaria (Lily of the valley) 6X, Crataegus (Hawthorn berries) 6X, Crataegus (Hawthorn flowers and leaves) 6X, Crocus sativus (Saffron) 6X, Digitalis (Foxglove) 6X, Equisetum (Common horsetail) 6X, Hypericum (St. Johns wort) 6X, Leonurus (Motherwort) 6X, Melissa (Lemon balm) 6X, Rosa (Garden rose) 6X, Rosmarinus (Rosemary) 6X, Ruta (Rue) 6X, Sanguisorba (Great burnet) 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Propolis

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

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

CordiaLiquidCordiaLiquid

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JD1
ARNICA MONTANA FLOWERACTIVE INGREDIENTOZ0E5Y15PZ1
CONVALLARIA MAJALISACTIVE INGREDIENTQHH4HVF5QE1
DIGITALISACTIVE INGREDIENTF1T8QT9U8B1
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65Z1
GOLDACTIVE INGREDIENT79Y1949PYO1
HAWTHORN LEAF WITH FLOWERACTIVE INGREDIENT6OM09RPY361
LEONURUS CARDIACA FLOWERING TOPACTIVE INGREDIENTIJ4SXX96Y41
MELISSA OFFICINALISACTIVE INGREDIENTYF70189L0N1
ROSMARINUS OFFICINALIS FLOWERING TOPACTIVE INGREDIENT8JM482TI791
RUTA GRAVEOLENS FLOWERING TOPACTIVE INGREDIENTN94C2U587S1
SAFFRONACTIVE INGREDIENTE849G4X5YJ1
SANGUINARIA CANADENSIS ROOTACTIVE INGREDIENTN9288CD5081
SEDUM ROSEUM WHOLEACTIVE INGREDIENTRH0WP583U31
SELENICEREUS GRANDIFLORUS STEMACTIVE INGREDIENT7114SV0MYK1
ST. JOHN'S WORTACTIVE INGREDIENTUFH8805FKA1
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JD1
ARNICA MONTANA FLOWERACTIVE MOIETYOZ0E5Y15PZ1
CONVALLARIA MAJALISACTIVE MOIETYQHH4HVF5QE1
DIGITALISACTIVE MOIETYF1T8QT9U8B1
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65Z1
GOLDACTIVE MOIETY79Y1949PYO1
HAWTHORN LEAF WITH FLOWERACTIVE MOIETY6OM09RPY361
LEONURUS CARDIACA FLOWERING TOPACTIVE MOIETYIJ4SXX96Y41
MELISSA OFFICINALISACTIVE MOIETYYF70189L0N1
ROSMARINUS OFFICINALIS FLOWERING TOPACTIVE MOIETY8JM482TI791
RUTA GRAVEOLENS FLOWERING TOPACTIVE MOIETYN94C2U587S1
SAFFRONACTIVE MOIETYE849G4X5YJ1
SANGUINARIA CANADENSIS ROOTACTIVE MOIETYN9288CD5081
SEDUM ROSEUM WHOLEACTIVE MOIETYRH0WP583U31
SELENICEREUS GRANDIFLORUS STEMACTIVE MOIETY7114SV0MYK1
ST. JOHN'S WORTACTIVE MOIETYUFH8805FKA1
PROPOLIS WAXINACTIVE INGREDIENT6Y8XYV2NOF1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-313148951-3131-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPOLIS WAX6Y8XYV2NOFIACT
ACONITUM NAPELLUSU0NQ8555JDACTIB
ARNICA MONTANA FLOWEROZ0E5Y15PZACTIB
GOLD79Y1949PYOACTIB
SELENICEREUS GRANDIFLORUS STEM7114SV0MYKACTIB
CONVALLARIA MAJALISQHH4HVF5QEACTIB
HAWTHORN LEAF WITH FLOWER6OM09RPY36ACTIB
SAFFRONE849G4X5YJACTIB
DIGITALISF1T8QT9U8BACTIB
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
ST. JOHN'S WORTUFH8805FKAACTIB
LEONURUS CARDIACA FLOWERING TOPIJ4SXX96Y4ACTIB
MELISSA OFFICINALISYF70189L0NACTIB
SEDUM ROSEUM WHOLERH0WP583U3ACTIB
ROSMARINUS OFFICINALIS FLOWERING TOP8JM482TI79ACTIB
RUTA GRAVEOLENS FLOWERING TOPN94C2U587SACTIB
WATER059QF0KO0RIACT
SANGUINARIA CANADENSIS ROOTN9288CD508ACTIB

Source Document#

Source XML · Source PDF

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
c48361b5-32b8-3154-e053-2a95a90a36838264753c-020b-46cb-959a-8397a03364112021-06-11WarningsExact identifier
spl set id: 8264753c-020b-46cb-959a-8397a0336411

Reported adverse events (FAERS/openFDA)#

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