Home DailyMed 28e670ca-ed35-4256-af20-74c25dc18099 Glyreg Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Deseret Biologicals, Inc | Apotheca Company
Effective date 2024-04-23
Label type HUMAN OTC DRUG LABEL
Version 3
Source full-release
Hydrated at 2026-06-01 02:26:43 Label at a glance# Product Glyreg
Active ingredient ACETIC ACID, COCOA, MAGNESIUM SULFATE HEPTAHYDRATE, SODIUM SULFATE, VERBASCUM THAPSUS WHOLE, SUS SCROFA ADRENAL GLAND, SUS SCROFA PANCREAS, CORTISONE ACETATE, THYROID, IODINE, LYCOPODIUM CLAVATUM SPORE, PHOSPHORUS, RANUNCULUS BULBOSUS WHOLE, SUCROSE, VANADIUM, ZINC, CHROMIUM TRIOXIDE, CULEX PIPIENS
Label structure 9 sections
Indications and uses • For the temporary relief of symptoms including: • hunger • self induced vertigo • brain fog • shakiness • fatigue • cravings • irritability These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Dosage and administration 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-1931-1 Glyreg 30 mL in 1 BOTTLE, DROPPER LIQUID 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-1931 GLYREG (ACETICUM ACIDUM, CACAO, MAGNESIA SULPHURICA, NATRUM SULPHURICUM, VERBASCUM THAPSUS, GLANDULA SUPRARENALIS SUIS, PANCREAS SUIS, CORTISONE ACETICUM, THYROIDINUM (SUIS), IODIUM, LYCOPODIUM CLAVATUM, PHOSPHORUS, RANUNCULUS BULBOSUS, SACCHARUM OFFICINALE, VANADIUM METALLICUM, ZINCUM METALLICUM, CHROMIUM ACIDUM, CULEX MUSCA) LIQUID [DESERET BIOLOGICALS, INC] 3 Current NDC, Legacy NDC, 1 package rows 20240425_28e670ca-ed35-4256-af20-74c25dc18099.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 28 matching rows.
Glyreg Aceticum Acidum, Cacao, Magnesia Sulphurica, Natrum Sulphuricum, Verbascum Thapsus, Glandula Suprarenalis Suis, Pancreas Suis, Cortisone Aceticum, Thyroidinum (Suis), Iodium, Lycopodium Clavatum, Phosphorus, Ranunculus Bulbosus, Saccharum Officinale, Vanadium Metallicum, Zincum Metallicum, Chromium Acidum, Culex Musca ACETIC ACID COCOA MAGNESIUM SULFATE HEPTAHYDRATE MAGNESIUM CATION SODIUM SULFATE SODIUM SULFATE ANHYDROUS VERBASCUM THAPSUS WHOLE VERBASCUM THAPSUS SUS SCROFA ADRENAL GLAND SUS SCROFA PANCREAS CORTISONE ACETATE CORTISONE THYROID SUS SCROFA THYROID IODINE LYCOPODIUM CLAVATUM SPORE PHOSPHORUS RANUNCULUS BULBOSUS WHOLE RANUNCULUS BULBOSUS SUCROSE VANADIUM ZINC CHROMIUM TRIOXIDE CULEX PIPIENS WATER ALCOHOL Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 20 matching rows.
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 Glyreg ACETICUM ACIDUM, CACAO, MAGNESIA SULPHURICA, NATRUM SULPHURICUM, VERBASCUM THAPSUS, GLANDULA SUPRARENALIS SUIS, PANCREAS SUIS, CORTISONE ACETICUM, THYROIDINUM (SUIS), IODIUM, LYCOPODIUM CLAVATUM, PHOSPHORUS, RANUNCULUS BULBOSUS, SACCHARUM OFFICINALE, VANADIUM METALLICUM, ZINCUM METALLICUM, CHROMIUM ACIDUM, CULEX MUSCA Deseret Biologicals, Inc 28e670ca-ed35-4256-af20-74c25dc18099 2024-04-23 Warnings Exact identifier ndc (package): 43742-1931-1 ndc (product): 43742-1931 ndc11 (package): 43742193101 spl id: c6f32d3a-1fc3-4ae3-bbcc-ed14daf67c9e spl set id: 28e670ca-ed35-4256-af20-74c25dc18099
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.