Cordia by Uriel Pharmacy Inc. CORDIA liquid

Cordia by

Drug Labeling and Warnings

Cordia by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION

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

ACTIVE INGREDIENT

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

Inactive Ingredients: Distilled water, Propolis

PURPOSE

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

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.

QUESTIONS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CORDIA 
cordia liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-3131
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	6 [hp_X]  in 1 mL
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (ARNICA MONTANA FLOWER - UNII:OZ0E5Y15PZ)	ARNICA MONTANA FLOWER	6 [hp_X]  in 1 mL
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	6 [hp_X]  in 1 mL
SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (SELENICEREUS GRANDIFLORUS STEM - UNII:7114SV0MYK)	SELENICEREUS GRANDIFLORUS STEM	6 [hp_X]  in 1 mL
CONVALLARIA MAJALIS (UNII: QHH4HVF5QE) (CONVALLARIA MAJALIS - UNII:QHH4HVF5QE)	CONVALLARIA MAJALIS	6 [hp_X]  in 1 mL
HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (HAWTHORN LEAF WITH FLOWER - UNII:6OM09RPY36)	HAWTHORN LEAF WITH FLOWER	6 [hp_X]  in 1 mL
SAFFRON (UNII: E849G4X5YJ) (SAFFRON - UNII:E849G4X5YJ)	SAFFRON	6 [hp_X]  in 1 mL
DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B)	DIGITALIS	6 [hp_X]  in 1 mL
EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z)	EQUISETUM ARVENSE TOP	6 [hp_X]  in 1 mL
ST. JOHN'S WORT (UNII: UFH8805FKA) (ST. JOHN'S WORT - UNII:UFH8805FKA)	ST. JOHN'S WORT	6 [hp_X]  in 1 mL
LEONURUS CARDIACA FLOWERING TOP (UNII: IJ4SXX96Y4) (LEONURUS CARDIACA FLOWERING TOP - UNII:IJ4SXX96Y4)	LEONURUS CARDIACA FLOWERING TOP	6 [hp_X]  in 1 mL
MELISSA OFFICINALIS (UNII: YF70189L0N) (MELISSA OFFICINALIS - UNII:YF70189L0N)	MELISSA OFFICINALIS	6 [hp_X]  in 1 mL
SEDUM ROSEUM WHOLE (UNII: RH0WP583U3) (SEDUM ROSEUM WHOLE - UNII:RH0WP583U3)	SEDUM ROSEUM WHOLE	6 [hp_X]  in 1 mL
ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79) (ROSMARINUS OFFICINALIS FLOWERING TOP - UNII:8JM482TI79)	ROSMARINUS OFFICINALIS FLOWERING TOP	6 [hp_X]  in 1 mL
RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S)	RUTA GRAVEOLENS FLOWERING TOP	6 [hp_X]  in 1 mL
SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508)	SANGUINARIA CANADENSIS ROOT	6 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-3131-3	60 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	09/01/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy Inc. (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy Inc.		043471163	manufacture(48951-3131)