Home NDC 44911-0722 Thyroid HP
Product NDC 44911-0722
11-digit product format 449110722
Labeler code 44911
Product ID 44911-0722_b7249b51-5056-4cd4-8912-6f51923118e6
Type HUMAN OTC DRUG
Nonproprietary name Baryta Carbonica, Calcarea Carbonica, Calcarea Iodata, Fucus Vesiculosus, Iodium, Lapis Albus, Levothyroxinum, Natrum Muriaticum, Pulsatilla (Vulgaris), Selenium Metallicum, Spongia Tosta, Thyroidinum (Suis)
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-09-30
Substance BARIUM CARBONATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM IODIDE; FUCUS VESICULOSUS; IODINE; CALCIUM HEXAFLUOROSILICATE; LEVOTHYROXINE; SODIUM CHLORIDE; PULSATILLA VULGARIS WHOLE; SELENIUM; SPONGIA OFFICINALIS SKELETON, ROASTED; THYROID
Active strength 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Thyroxine [CS], l-Thyroxine [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Thyroid HP
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BARIUM CARBONATE 30 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL CALCIUM IODIDE 30 [hp_X]/mL FUCUS VESICULOSUS 30 [hp_X]/mL IODINE 30 [hp_X]/mL CALCIUM HEXAFLUOROSILICATE 30 [hp_X]/mL LEVOTHYROXINE 30 [hp_X]/mL SODIUM CHLORIDE 30 [hp_X]/mL PULSATILLA VULGARIS WHOLE 30 [hp_X]/mL SELENIUM 30 [hp_X]/mL SPONGIA OFFICINALIS SKELETON, ROASTED 30 [hp_X]/mL THYROID 30 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0722-1 Thyroid HP 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0722 THYROID HP (BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA IODATA, FUCUS VESICULOSUS, IODIUM, LAPIS ALBUS, LEVOTHYROXINUM, NATRUM MURIATICUM, PULSATILLA (VULGARIS), SELENIUM METALLICUM, SPONGIA TOSTA, THYROIDINUM (SUIS)) LIQUID [ENERGIQUE, INC.] 1 Current NDC, 1 package rows 20241024_2f04e425-7160-41a7-aa1e-934db54f1751.zip
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 Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Thyroid HP BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA IODATA, FUCUS VESICULOSUS, IODIUM, LAPIS ALBUS, LEVOTHYROXINUM, NATRUM MURIATICUM, PULSATILLA (VULGARIS), SELENIUM METALLICUM, SPONGIA TOSTA, THYROIDINUM (SUIS) Energique, Inc. 2f04e425-7160-41a7-aa1e-934db54f1751 2024-09-30 Warnings Exact identifier ndc (product): 44911-0722
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 44911-0722-1 44911072201 30 mL in 1 BOTTLE, DROPPER (44911-0722-1) 30 ml 2024-09-30 No No Current