FDA.reportPublic FDA data

Thuja Thymus comp

Manufacturer
Uriel Pharmacy Inc.
Effective date
2021-05-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:35

Label at a glance#

ProductThuja Thymus comp.
Active ingredientFORMICA RUFA, PORK KIDNEY, LEVISTICUM OFFICINALE ROOT, THUJA OCCIDENTALIS WHOLE, AMANITA MUSCARIA FRUITING BODY, EQUISETUM ARVENSE TOP, ACTIVATED CHARCOAL, SLOE, URTICA DIOICA, ASPLENIUM SCOLOPENDRIUM TOP, SILVER, MERCURY, DRYOPTERIS FILIX-MAS ROOT, PTERIDIUM AQUILINUM WHOLE, SILICON DIOXIDE, BEEF LIVER, BOS TAURUS THYMUS, OSTREA EDULIS SHELL
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

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

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Equisetum (Common horsetail) 2X, Levisticum (Lovage) 2X, Prunus spinosa (Blackthorn) 2X, Urtica dioica (Stinging nettle) 2X, Filix mas (Male fern) 3X, Pteridium aquil. (Eagle fern) 3X, Scolopendrium (Hart’s tongue) 3X, Hepar (Bovine liver) 4X, Gland. thymus (Bovine thymus) 4X, Conchae (Oyster shells) 5X, Formica (Red wood ant) 5X, Argentum (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: Distilled water, 20% Organic cane alcohol, Lactose

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. 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
Made with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Thuja Thymus comp LiquidThuja Thymus comp Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9363-3Thuja Thymus comp.60 mL in 1 BOTTLE, DROPPERLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9363THUJA THYMUS COMP. (THUJA THYMUS COMP) LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20210603_c3697270-e230-97b8-e053-2995a90ae572.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-936348951-9363-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
FORMICA RUFA55H0W83JO5ACTIB
PORK KIDNEYX7BCI5P86HACTIB
ALCOHOL3K9958V90MIACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
LEVISTICUM OFFICINALE ROOT46QZ19OEX8ACTIB
THUJA OCCIDENTALIS WHOLE5HBV6WCE3NACTIB
AMANITA MUSCARIA FRUITING BODYDIF093I037ACTIB
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
SLOE3MLB4858X7ACTIB
URTICA DIOICA710FLW4U46ACTIB
ASPLENIUM SCOLOPENDRIUM TOPHJA3YWQ7HLACTIB
SILVER3M4G523W1GACTIB
MERCURYFXS1BY2PGLACTIB
DRYOPTERIS FILIX-MAS ROOTC0ZK0RRF5XACTIB
PTERIDIUM AQUILINUM WHOLE05T3M06HCMACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
BEEF LIVERW8N8R55022ACTIB
BOS TAURUS THYMUS8XEJ88V2T8ACTIB
OSTREA EDULIS SHELL49OY13BE7ZACTIB
WATER059QF0KO0RIACT

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
c3697270-e231-97b8-e053-2995a90ae572c3697270-e230-97b8-e053-2995a90ae5722021-05-28WarningsExact identifier
spl id: c3697270-e231-97b8-e053-2995a90ae572
spl set id: c3697270-e230-97b8-e053-2995a90ae572

Reported adverse events (FAERS/openFDA)#

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