FDA.reportPublic FDA data

Mandragora Arnica

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-11-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:28:51

Label at a glance#

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

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

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 (Redwood ant) 10X, Arnica 15X, Equisetum (Common horsetail) 15X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Organic sucrose

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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. 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.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mandragora Arnica PelletsMandragora Arnica Pellets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8416-2Mandragora Arnica1350 in 1 BOTTLE, GLASSPELLET13501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8416MANDRAGORA ARNICA PELLET [URIEL PHARMACY INC.]11 package rows20241109_266abdc4-3fb3-3d05-e063-6394a90a6e15.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-841648951-8416-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
BETULA PUBESCENS LEAF84SOH0O3OOACTIB
MANDRAGORA OFFICINARUM ROOTI2XCB174VBACTIB
SUS SCROFA MENISCUS1C8T78BD9QACTIB
FORMICA RUFA55H0W83JO5ACTIB
ARNICA MONTANAO80TY208ZWACTIB
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB

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
266a9d69-b1cc-9405-e063-6294a90ac8fa266abdc4-3fb3-3d05-e063-6394a90a6e152024-11-08WarningsExact identifier
spl id: 266a9d69-b1cc-9405-e063-6294a90ac8fa
spl set id: 266abdc4-3fb3-3d05-e063-6394a90a6e15

Reported adverse events (FAERS/openFDA)#

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