FDA.reportPublic FDA data

Thyreoidea Ferrum

Manufacturer
Uriel Pharmacy Inc.
Effective date
2019-10-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:06:10

Label at a glance#

ProductThyreoidea Ferrum
Active ingredientTHYROID, UNSPECIFIED, FUCUS VESICULOSUS, URTICA DIOICA, FERROUS ARSENATE, IRON
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: Fucus ves. (Bladderweed) 3X, Glandula thyreoidea (Bovine thyroid gland) 3X, Urtica dioica (Stinging nettle) 3X, Ferrum arsenicosum (Iron arsenite solution) 6X, Ferrum sidereum (Meteoric iron) 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic sucrose, 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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Contains traces of lactose. 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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Thyreoidea Ferrum PelletsThyreoidea Ferrum Pellets

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
48951-935348951-9353-2

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
THYROID, UNSPECIFIED0B4FDL9I6PACTIB
FUCUS VESICULOSUS535G2ABX9MACTIB
URTICA DIOICA710FLW4U46ACTIB
FERROUS ARSENATE129CO35H12ACTIB
IRONE1UOL152H7ACTIB
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT

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
213aa38e-b6ce-cab4-e063-6394a90a3c3d94f666ae-d62a-2f79-e053-2a95a90ad4022024-09-03WarningsExact identifier
spl set id: 94f666ae-d62a-2f79-e053-2a95a90ad402

Reported adverse events (FAERS/openFDA)#

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