FDA.reportPublic FDA data

SLOE

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-01-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:25:40

Label at a glance#

ProductThuja Thymus comp.
Active ingredientSLOE, DRYOPTERIS FILIX-MAS ROOT, PTERIDIUM AQUILINUM WHOLE, URTICA DIOICA, BOS TAURUS THYMUS, BEEF LIVER, THUJA OCCIDENTALIS WHOLE, PORK KIDNEY, ASPLENIUM SCOLOPENDRIUM TOP, OSTREA EDULIS SHELL, SILVER, SILICON DIOXIDE, MERCURY, ACTIVATED CHARCOAL, FORMICA RUFA, AMANITA MUSCARIA FRUITING BODY, EQUISETUM ARVENSE TOP, LEVISTICUM OFFICINALE ROOT
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: Equisetum (Common horsetail) 2X, Levisticum (Lovage) 2X, Prunus spin. (Blackthorn) 2X, Urtica dioica (Stinging nettle) 2X, Filix (Male fern) 3X, Pteridium (Eagle fern) 3X, Scolopendrium (Hart's tongue) 3X, Formica (Red wood ant) 4X, Gland. thymus (Bovine thymus) 4X, Hepar (Bovine liver) 4X, Conchae (Oyster shells) 5X, Argentum met. (Silver) 6X, Renes (Bovine kidneys) 6X, Thuja (American arborvitae) 6X, Agaricus (Fly agaric mushroom) 7X, Quartz (Rock crystal) 12X, Mercurius vivus (Mercury) 14X, Carbo betula (Birch wood charcoal) 20X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic sucrose, Lactose

"prepared using rhythmical processes"

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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use.Do not use if allergic to any ingredient. Contains traces of lactose. 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

Thuja thymus comp pelletsThuja thymus comp pellets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9362-2Thuja Thymus comp.1350 in 1 BOTTLE, GLASSPELLET13502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9362THUJA THYMUS COMP. PELLET [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20240116_c3688cef-dc4f-3c4c-e053-2995a90af2d8.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-936248951-9362-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
SLOE3MLB4858X7ACTIB
DRYOPTERIS FILIX-MAS ROOTC0ZK0RRF5XACTIB
PTERIDIUM AQUILINUM WHOLE05T3M06HCMACTIB
URTICA DIOICA710FLW4U46ACTIB
BOS TAURUS THYMUS8XEJ88V2T8ACTIB
BEEF LIVERW8N8R55022ACTIB
THUJA OCCIDENTALIS WHOLE5HBV6WCE3NACTIB
PORK KIDNEYX7BCI5P86HACTIB
ASPLENIUM SCOLOPENDRIUM TOPHJA3YWQ7HLACTIB
OSTREA EDULIS SHELL49OY13BE7ZACTIB
SILVER3M4G523W1GACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
MERCURYFXS1BY2PGLACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
SUCROSEC151H8M554IACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
FORMICA RUFA55H0W83JO5ACTIB
AMANITA MUSCARIA FRUITING BODYDIF093I037ACTIB
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
LEVISTICUM OFFICINALE ROOT46QZ19OEX8ACTIB

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
0f00778e-bb36-e0d3-e063-6394a90a5e77c3688cef-dc4f-3c4c-e053-2995a90af2d82024-01-15WarningsExact identifier
spl id: 0f00778e-bb36-e0d3-e063-6394a90a5e77
spl set id: c3688cef-dc4f-3c4c-e053-2995a90af2d8

Reported adverse events (FAERS/openFDA)#

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