Chemtox

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Chemtox
Generic name: TRITICUM AESTIVUM, BERBERIS VULGARIS, GLYCYRRHIZA GLABRA, LAPPA MAJOR, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, XANTHOXYLUM FRAXINEUM, PHYTOLACCA DECANDRA, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, LYMPH NODE (SUIS), THYROIDINUM (SUIS), BELLADONNA, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM, PHOSPHORUS, SALICYLICUM ACIDUM, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE,
Manufacturer: BioActive Nutritional, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: a480e5f4-5f9e-4b23-b257-b0ac1ebfc115
SPL ID: a7970fbd-67d5-4fc7-b49f-bff4f3430045
Version: 1
Effective date: 2025-01-07
Source export date: 2026-11-06
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:53:55

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 2 · 48 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Chemtox	openfda.brand_name
generic name		TRITICUM AESTIVUM, BERBERIS VULGARIS, GLYCYRRHIZA GLABRA, LAPPA MAJOR, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, XANTHOXYLUM FRAXINEUM, PHYTOLACCA DECANDRA, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, LYMPH NODE (SUIS), THYROIDINUM (SUIS), BELLADONNA, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM, PHOSPHORUS, SALICYLICUM ACIDUM, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE,	openfda.generic_name
manufacturer name		BioActive Nutritional, Inc.	openfda.manufacturer_name
ndc	package	43857-0654-1	openfda.package_ndc
ndc	product	43857-0654	openfda.product_ndc
ndc11	package	43857065401	derived:openfda.package_ndc
spl id		a7970fbd-67d5-4fc7-b49f-bff4f3430045	id
spl set id		a480e5f4-5f9e-4b23-b257-b0ac1ebfc115	set_id
unii		27YLU75U4W	openfda.unii
unii		6RV024OAUQ	openfda.unii
unii		11E6VI8VEG	openfda.unii
unii		2788Z9758H	openfda.unii
unii		A4KL1HMZ7T	openfda.unii
unii		VCQ006KQ1E	openfda.unii
unii		269XH13919	openfda.unii
unii		3C3Y389JBU	openfda.unii
unii		8CRQ2TH63M	openfda.unii
unii		R57ZHV85D4	openfda.unii
unii		4T6H12BN9U	openfda.unii
unii		883WKN7W8X	openfda.unii
unii		S2D77IH61R	openfda.unii
unii		1VPU26JZZ4	openfda.unii
unii		4R7X1O2820	openfda.unii
unii		411VRN1TV4	openfda.unii
unii		O414PZ4LPZ	openfda.unii
unii		8SKN0B0MIM	openfda.unii
unii		1TH8Q20J0U	openfda.unii
unii		4VBP01X99F	openfda.unii
unii		Q40Q9N063P	openfda.unii
unii		3T8H1794QW	openfda.unii
unii		33A7VYU29L	openfda.unii
unii		K0U68Q2TXA	openfda.unii
unii		LKG8494WBH	openfda.unii
unii		GN5P7K3T8S	openfda.unii
unii		YUL4LO94HK	openfda.unii
unii		2DI9HA706A	openfda.unii
unii		3B8D35Y7S4	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		398IYQ16YV	openfda.unii
unii		2P299V784P	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.