Arnica Cordifolia Essence

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-05-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:10:19

Label at a glance#

ProductArnica Cordifolia Essence
Active ingredientARNICA CORDIFOLIA WHOLE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

FOR EXTERNAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Directions: For compresses: Use 2 teaspoons per
cup of lukewarm water. For full bath: Use 2-3 tablespoons.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Arnica cordifolia recens e planta tota 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 20% Organic cane alcohol

OTC - PURPOSE SECTION

Uses: Temporary relief of bruises and sprains.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: FOR EXTERNAL USE ONLY.
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, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. 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
www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArnicaCordifoliaEssenceArnicaCordifoliaEssence

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1289-6Arnica Cordifolia Essence125 mL in 1 BOTTLE, GLASSLIQUID1251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1289ARNICA CORDIFOLIA ESSENCE LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20180614_6b3f6c79-1b8e-3bf3-e053-2991aa0a3fc1.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-128948951-1289-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
ARNICA CORDIFOLIA WHOLE82CNE9JKJIACTIB

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
6b3f6c79-1b8f-3bf3-e053-2991aa0a3fc16b3f6c79-1b8e-3bf3-e053-2991aa0a3fc12018-05-02WarningsExact identifier
spl id: 6b3f6c79-1b8f-3bf3-e053-2991aa0a3fc1
spl set id: 6b3f6c79-1b8e-3bf3-e053-2991aa0a3fc1

Reported adverse events (FAERS/openFDA)#

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