Thyropar

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2023-10-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:22:56

Label at a glance#

ProductThyropar
Active ingredientFUCUS VESICULOSUS, SPONGIA OFFICINALIS SKELETON, ROASTED, SUS SCROFA ADRENAL GLAND, SUS SCROFA PITUITARY GLAND, SUS SCROFA THYROID, BROMINE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, IODINE, LACHESIS MUTA VENOM, ANEMONE PRATENSIS
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 12.48% of Bromium 12X, Calcarea Carbonica 12X, Glandula Suprarenalis (Suis) 6X, Hypophysis Suis 6X, Iodium 12X, Lachesis Mutus 12X, Pulsatilla (Pratensis) 12X, Thyroidinum (Suis) 6X; 0.10% of Fucus Vesiculosus 3X, Spongia Tosta 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve exhaustion and heaviness of the body, dry rough skin, dry cough, difficulty swallowing and swollen throat.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve exhaustion and heaviness of the body, dry rough skin, dry cough, difficulty swallowing and swollen throat.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 20% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579 800.869.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE
SINCE 1987
HOMEOPATHIC REMEDY
THYROPAR
1 fl. oz. (30 ml)

ThyroparThyropar

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0535-12023-10-30C16284748780-1d6a99b39-87ab-a426-e053-dadaa90af4c2Drug Facts:
44911-0535-12022-01-28C16284748780-1d6a99b39-87ab-a426-e053-dadaa90af4c2Drug Facts:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0535-1Thyropar30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0535THYROPAR (FUCUS VESICULOSUS, SPONGIA TOSTA, GLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, THYROIDINUM (SUIS), BROMIUM, CALCAREA CARBONICA, IODIUM, LACHESIS MUTUS, PULSATILLA (PRATENSIS)) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20231031_9482ff15-15b2-4c1f-ae15-24f6d810254e.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
44911-053544911-0535-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
ThyroparFUCUS VESICULOSUS, SPONGIA TOSTA, GLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, THYROIDINUM (SUIS), BROMIUM, CALCAREA CARBONICA, IODIUM, LACHESIS MUTUS, PULSATILLA (PRATENSIS)Energique, Inc.9482ff15-15b2-4c1f-ae15-24f6d810254e2023-10-30WarningsExact identifier
ndc (package): 44911-0535-1
ndc (product): 44911-0535
ndc11 (package): 44911053501
spl id: 1387214b-6ef9-4562-aa90-3a7c31bd7c61
spl set id: 9482ff15-15b2-4c1f-ae15-24f6d810254e

Reported adverse events (FAERS/openFDA)#

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