FDA.reportPublic FDA data

Mandragora Arnica

Manufacturer
Uriel Pharmacy, Inc.
Effective date
2024-11-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:28:54

Label at a glance#

ProductMandragora Arnica
Active ingredientARNICA MONTANA WHOLE, BETULA PUBESCENS LEAF, MANDRAGORA OFFICINARUM ROOT, EQUISETUM ARVENSE TOP, FORMICA RUFA, SUS SCROFA MENISCUS
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE.

DOSAGE & ADMINISTRATION SECTION

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Betula (Silver birch leaves) 3X, Mandragora (Mandrake) 3X, Meniscus genus (Bovine medial meniscus of the knee joint) 8X, Formica (Red wood ant) 10X, Arnica 15X, Equisetum (Common horsetail) 15X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of sore joints.

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.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mandragora Arnica AmpulesMandragora Arnica Ampules

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-7200-1Mandragora Arnica10 in 1 BOXLIQUID102
48951-7200-1Mandragora Arnica1 mL in 1 AMPULELIQUID12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7200MANDRAGORA ARNICA LIQUID [URIEL PHARMACY, INC.]2Legacy NDC, 2 package rows20241115_dfb07548-ba82-15bb-e053-2a95a90a5043.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-720048951-7200-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARNICA MONTANA WHOLEO80TY208ZWACTIB
WATER059QF0KO0RIACT
BETULA PUBESCENS LEAF84SOH0O3OOACTIB
MANDRAGORA OFFICINARUM ROOTI2XCB174VBACTIB
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
SODIUM CHLORIDE451W47IQ8XIACT
FORMICA RUFA55H0W83JO5ACTIB
SUS SCROFA MENISCUS1C8T78BD9QACTIB

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
26d18b42-612f-43b6-e063-6394a90a5f4ddfb07548-ba82-15bb-e053-2a95a90a50432024-11-13WarningsExact identifier
spl id: 26d18b42-612f-43b6-e063-6394a90a5f4d
spl set id: dfb07548-ba82-15bb-e053-2a95a90a5043

Reported adverse events (FAERS/openFDA)#

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