Home NDC 43742-1416 Chemtox
Product NDC 43742-1416
11-digit product format 437421416
Labeler code 43742
Product ID 43742-1416_9a438406-8bcd-4997-b4d9-c02f7aa7dcf6
Type HUMAN OTC DRUG
Nonproprietary name Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Hepar Suis, Phytolacca Decandra, Glandula Suprarenalis Suis, Thyroidinum (Suis), Arsenicum Album, Asarum Canadense, Carbolicum Acidum, Carboneum Sulphuratum, Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphorus, Selenium Metallicum, Sulphuricum Acidum, Chlorinum, Butylbenzene, Petroleum, Sorbitol
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-01-02
Substance BERBERIS VULGARIS ROOT BARK; GLYCYRRHIZA GLABRA; ARCTIUM LAPPA ROOT; STILLINGIA SYLVATICA ROOT; TRIFOLIUM PRATENSE FLOWER; PORK LIVER; PHYTOLACCA AMERICANA ROOT; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYROID; ARSENIC TRIOXIDE; ASARUM CANADENSE ROOT; PHENOL; CARBON DISULFIDE; IRIDIUM; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; SELENIUM; SULFURIC ACID; CHLORINE; BUTYLBENZENE; KEROSENE; SORBITOL
Active strength 3; 3; 3; 3; 3; 8; 8; 8; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 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; [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], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS]
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 Chemtox
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL GLYCYRRHIZA GLABRA 3 [hp_X]/mL ARCTIUM LAPPA ROOT 3 [hp_X]/mL STILLINGIA SYLVATICA ROOT 3 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL PORK LIVER 8 [hp_X]/mL PHYTOLACCA AMERICANA ROOT 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL SUS SCROFA THYROID 8 [hp_X]/mL ARSENIC TRIOXIDE 12 [hp_X]/mL ASARUM CANADENSE ROOT 12 [hp_X]/mL PHENOL 12 [hp_X]/mL CARBON DISULFIDE 12 [hp_X]/mL IRIDIUM 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL NITRIC ACID 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL PHOSPHORUS 12 [hp_X]/mL SELENIUM 12 [hp_X]/mL SULFURIC ACID 12 [hp_X]/mL CHLORINE 12 [hp_X]/mL BUTYLBENZENE 30 [hp_X]/mL KEROSENE 30 [hp_X]/mL SORBITOL 30 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 2 · 24 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 43742-1416-1 Chemtox 30 mL in 1 BOTTLE, DROPPER LIQUID 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-1416 CHEMTOX (BERBERIS VULGARIS, GLYCYRRHIZA GLABRA, LAPPA MAJOR, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, HEPAR SUIS, PHYTOLACCA DECANDRA, GLANDULA SUPRARENALIS SUIS, THYROIDINUM (SUIS), ARSENICUM ALBUM, ASARUM CANADENSE, CARBOLICUM ACIDUM, CARBONEUM SULPHURATUM, IRIDIUM METALLICUM, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORUS, SELENIUM METALLICUM, SULPHURICUM ACIDUM, CHLORINUM, BUTYLBENZENE, PETROLEUM, SORBITOL) LIQUID [DESERET BIOLOGICALS, INC.] 5 Current NDC, Legacy NDC, 1 package rows 20240308_91f52c95-f36d-4754-8570-f81ed8d36180.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 Chemtox BERBERIS VULGARIS, GLYCYRRHIZA GLABRA, LAPPA MAJOR, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, HEPAR SUIS, PHYTOLACCA DECANDRA, GLANDULA SUPRARENALIS SUIS, THYROIDINUM (SUIS), ARSENICUM ALBUM, ASARUM CANADENSE, CARBOLICUM ACIDUM, CARBONEUM SULPHURATUM, IRIDIUM METALLICUM, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORUS, SELENIUM METALLICUM, SULPHURICUM ACIDUM, CHLORINUM, BUTYLBENZENE, PETROLEUM, SORBITOL Deseret Biologicals, Inc. 91f52c95-f36d-4754-8570-f81ed8d36180 2024-03-06 Warnings Exact identifier ndc (product): 43742-1416
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-1416-1 43742141601 30 mL in 1 BOTTLE, DROPPER (43742-1416-1) 30 ml 2019-01-02 0000-00-00 No No Current