Home NDC 43742-1257 Bio Glyoxal Phase
Product NDC 43742-1257
11-digit product format 437421257
Labeler code 43742
Product ID 43742-1257_03d71963-e6ad-4b8d-9563-baff77787b37
Type HUMAN OTC DRUG
Nonproprietary name Arnica Montana, Baptisia Tinctoria, Echinacea (Angustifolia), Sanguinaria Canadensis, Eupatorium Perfoliatum, Euphorbium Officinarum, Dopamine Hydrochloride, Phytolacca Decandra, Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Bryonia (Alba), Gelsemium Sempervirens, Mercurius Corrosivus, Phosphorus, Pulsatilla (Pratensis), Rhus Tox, Sulphur, Thuja Occidentalis, Cortisone Aceticum, Acetaldehyde, Formalinum, Hepar Sulphuris Calcareum, Lachesis Mutus, Zincum Metallicum
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-06-07
Substance ACETALDEHYDE; ACONITUM NAPELLUS WHOLE; ARNICA MONTANA WHOLE; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; CALCIUM SULFIDE; CORTISONE ACETATE; DOPAMINE HYDROCHLORIDE; ECHINACEA ANGUSTIFOLIA WHOLE; EUPATORIUM PERFOLIATUM FLOWERING TOP; EUPHORBIA RESINIFERA RESIN; FORMALDEHYDE; GELSEMIUM SEMPERVIRENS ROOT; LACHESIS MUTA VENOM; MERCURIC CHLORIDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PULSATILLA PRATENSIS WHOLE; SANGUINARIA CANADENSIS ROOT; SILVER NITRATE; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF; ZINC
Active strength 10; 8; 4; 8; 4; 8; 10; 8; 6; 5; 6; 6; 10; 8; 10; 8; 8; 7; 8; 5; 8; 8; 8; 8; 10 [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; [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 Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Bio Glyoxal Phase
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA WHOLE 10 [hp_X]/mL BAPTISIA TINCTORIA ROOT 8 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE 4 [hp_X]/mL SANGUINARIA CANADENSIS ROOT 8 [hp_X]/mL EUPATORIUM PERFOLIATUM FLOWERING TOP 4 [hp_X]/mL EUPHORBIA RESINIFERA RESIN 8 [hp_X]/mL DOPAMINE HYDROCHLORIDE 10 [hp_X]/mL PHYTOLACCA AMERICANA ROOT 8 [hp_X]/mL ACONITUM NAPELLUS WHOLE 6 [hp_X]/mL SILVER NITRATE 5 [hp_X]/mL ARSENIC TRIOXIDE 6 [hp_X]/mL BRYONIA ALBA ROOT 6 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT 10 [hp_X]/mL MERCURIC CHLORIDE 8 [hp_X]/mL PHOSPHORUS 10 [hp_X]/mL PULSATILLA PRATENSIS WHOLE 8 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF 8 [hp_X]/mL SULFUR 7 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG 8 [hp_X]/mL CORTISONE ACETATE 5 [hp_X]/mL ACETALDEHYDE 8 [hp_X]/mL FORMALDEHYDE 8 [hp_X]/mL CALCIUM SULFIDE 8 [hp_X]/mL LACHESIS MUTA VENOM 8 [hp_X]/mL ZINC 10 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 2 · 25 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 43742-1257-1 Bio Glyoxal Phase 30 mL in 1 BOTTLE, DROPPER LIQUID 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-1257 BIO GLYOXAL PHASE (ARNICA MONTANA, BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), SANGUINARIA CANADENSIS, EUPATORIUM PERFOLIATUM, EUPHORBIUM OFFICINARUM, DOPAMINE HYDROCHLORIDE, PHYTOLACCA DECANDRA, ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, BRYONIA (ALBA), GELSEMIUM SEMPERVIRENS, MERCURIUS CORROSIVUS, PHOSPHORUS, PULSATILLA (PRATENSIS), RHUS TOX, SULPHUR, THUJA OCCIDENTALIS, CORTISONE ACETICUM, ACETALDEHYDE, FORMALINUM, HEPAR SULPHURIS CALCAREUM, LACHESIS MUTUS, ZINCUM METALLICUM) LIQUID [DESERET BIOLOGICALS, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20240510_d43db203-7756-43a5-bd68-aa070d429f60.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 Bio Glyoxal Phase ARNICA MONTANA, BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), SANGUINARIA CANADENSIS, EUPATORIUM PERFOLIATUM, EUPHORBIUM OFFICINARUM, DOPAMINE HYDROCHLORIDE, PHYTOLACCA DECANDRA, ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, BRYONIA (ALBA), GELSEMIUM SEMPERVIRENS, MERCURIUS CORROSIVUS, PHOSPHORUS, PULSATILLA (PRATENSIS), RHUS TOX, SULPHUR, THUJA OCCIDENTALIS, CORTISONE ACETICUM, ACETALDEHYDE, FORMALINUM, HEPAR SULPHURIS CALCAREUM, LACHESIS MUTUS, ZINCUM METALLICUM Deseret Biologicals, Inc. d43db203-7756-43a5-bd68-aa070d429f60 2024-05-09 Warnings Exact identifier ndc (product): 43742-1257
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-1257-1 43742125701 30 mL in 1 BOTTLE, DROPPER (43742-1257-1) 30 ml 2019-06-07 0000-00-00 No No Current