Home NDC 43857-0614 Thyroplex
Product NDC 43857-0614
11-digit product format 438570614
Labeler code 43857
Product ID 43857-0614_6b7ef05b-8ab5-4f8f-9b25-8311411becd2
Type HUMAN OTC DRUG
Nonproprietary name Fucus Vesiculosus, Spongia Tosta, Iodium, Pulsatilla (Vulgaris), Glandula Suprarenalis Suis, Hypophysis Suis, Thyroidinum (Suis), Levothyroxinum, Calcarea Carbonica, Ferrum Iodatum, Kali Iodatum, Lycopus Virginicus, Phosphoricum Acidum
Dosage form LIQUID
Route ORAL
Labeler BioActive Nutritional
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-07-29
Substance FUCUS VESICULOSUS; SPONGIA OFFICINALIS SKELETON, ROASTED; IODINE; PULSATILLA VULGARIS WHOLE; SUS SCROFA ADRENAL GLAND; SUS SCROFA PITUITARY GLAND; THYROID; LEVOTHYROXINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; FERROUS IODIDE; POTASSIUM IODIDE; LYCOPUS VIRGINICUS WHOLE; PHOSPHORIC ACID
Active strength 3; 3; 6; 6; 8; 8; 8; 10; 12; 12; 12; 12; 12 [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; [hp_X]/mL
Pharmacologic classes Thyroxine [CS], l-Thyroxine [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
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 Thyroplex
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FUCUS VESICULOSUS 3 [hp_X]/mL SPONGIA OFFICINALIS SKELETON, ROASTED 3 [hp_X]/mL IODINE 6 [hp_X]/mL PULSATILLA VULGARIS WHOLE 6 [hp_X]/mL SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL SUS SCROFA PITUITARY GLAND 8 [hp_X]/mL THYROID 8 [hp_X]/mL LEVOTHYROXINE 10 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL FERROUS IODIDE 12 [hp_X]/mL POTASSIUM IODIDE 12 [hp_X]/mL LYCOPUS VIRGINICUS WHOLE 12 [hp_X]/mL PHOSPHORIC ACID 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 13 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43857-0614-1 Thyroplex 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43857-0614 THYROPLEX (FUCUS VESICULOSUS, SPONGIA TOSTA, IODIUM, PULSATILLA (VULGARIS), GLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, THYROIDINUM (SUIS), LEVOTHYROXINUM, CALCAREA CARBONICA, FERRUM IODATUM, KALI IODATUM, LYCOPUS VIRGINICUS, PHOSPHORICUM ACIDUM) LIQUID [BIOACTIVE NUTRITIONAL] 2 Current NDC, Legacy NDC, 1 package rows 20231014_977b06c5-e861-4cc4-ac56-1a960276bb85.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 Thyroplex FUCUS VESICULOSUS, SPONGIA TOSTA, IODIUM, PULSATILLA (VULGARIS), GLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, THYROIDINUM (SUIS), LEVOTHYROXINUM, CALCAREA CARBONICA, FERRUM IODATUM, KALI IODATUM, LYCOPUS VIRGINICUS, PHOSPHORICUM ACIDUM BioActive Nutritional 977b06c5-e861-4cc4-ac56-1a960276bb85 2026-06-08 Warnings Exact identifier ndc (product): 43857-0614
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43857-0614-1 43857061401 30 mL in 1 BOTTLE, DROPPER (43857-0614-1) 30 ml 2021-07-29 0000-00-00 No No Current