FDA.reportPublic FDA data

MetX

Manufacturer
Homeocare Laboratories Inc.
Effective date
2016-03-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:07:32

Label at a glance#

ProductMetX
Active ingredientTHYROID, UNSPECIFIED, FUCUS SERRATUS, TRIBASIC CALCIUM PHOSPHATE, GRAPHITE, SODIUM SULFIDE, LYCOPODIUM CLAVATUM SPORE, SUS SCROFA PLACENTA, ANTIMONY TRISULFIDE, BOS TAURUS HYPOTHALAMUS
Label structure9 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

PURPOSE

Appetite Control

Fatigue

Tendency to obesity

Weight control

Appetite disorders

Excessive appetite

water retention

Stress

Lack of energy

Metabolic disturbances

INDICATIONS & USAGE SECTION

USAGE AND DIRECTIONS


Adults

Take 12 drops 3 times per day under tongue 15 minutes before or after meal

Allow to remain in mouth for 60 seconds before swallowing

WARNINGS SECTION

WARNING

Ask a doctor befre use if you have known medical conditions,

pregnant or breastfeeding

Do not take if safety seal is broken

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

OTC - QUESTIONS SECTION

QUESTIONS AND COMMENTS

CALL - (520) 881-0440

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT

Antimonium crudum

Calcarea phos

Fucus

Graphites

Hypothalamus

Lycopodium

Natrum sulph

Nux vomica

Placenta suis

Thyroidinum

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT

Ethanol

Purified Water

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATION

Adults
Take 12 drops 3 times per day under tongue 15 minutes before or after meal
Allow to remain in mouth for 60 seconds before swallowing

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABELLABEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61727-001-002020-01-31C16284748780-19d75b9d0-5e93-f424-e053-dadaa90a57ce2814761c-0f3d-32cb-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61727-001-00MetX1 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61727-001METX SOLUTION/ DROPS [HOMEOCARE LABORATORIES INC.]5Legacy NDC, 1 package rows20160307_2814761c-0f3d-32cb-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61727-00161727-001-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
THYROID, UNSPECIFIED0B4FDL9I6PACTIB
FUCUS SERRATUSV8K40WNW5BACTIB
TRIBASIC CALCIUM PHOSPHATE91D9GV0Z28ACTIM
GRAPHITE4QQN74LH4OACTIB
SODIUM SULFIDEYGR27ZW0Y7ACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
SUS SCROFA PLACENTAC8CV8867O8ACTIB
ANTIMONY TRISULFIDEF79059A38UACTIB
BOS TAURUS HYPOTHALAMUSS6G2NLH4Y7ACTIB
1-(4-CHLOROPHENYL)-1-PHENYLETHANOL6149LO684BIACT
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
2d7816a3-05f7-224f-e054-00144ff88e882814761c-0f3d-32cb-e054-00144ff88e882016-03-07WarningsExact identifier
spl id: 2d7816a3-05f7-224f-e054-00144ff88e88
spl set id: 2814761c-0f3d-32cb-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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