Detoxifier

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: Detoxifier
Generic name: URICUM ACIDUM, BENZOICUM ACIDUM, BERBER. VULG., BRYONIA, CANTHARIS, CARDUUS BENEDICTUS, CEANOTHUS, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICA, CINCHONA, DIOSCOREA, DOLICHOS, IRIS VERSICOLOR, JUNIPERUS COM., NUX VOM.,PTELEA,TARAXACUM, CARDUUS MAR., CYNARA SCOLYMUS, SOLIDAGO
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 92ad49e0-2cfe-7d51-e053-2995a90a16f5
SPL ID: b4e1c678-878e-07b1-e053-2a95a90a909e
Version: 3
Effective date: 2020-11-24
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:27:08

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 1 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Detoxifier	openfda.brand_name
generic name		URICUM ACIDUM, BENZOICUM ACIDUM, BERBER. VULG., BRYONIA, CANTHARIS, CARDUUS BENEDICTUS, CEANOTHUS, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICA, CINCHONA, DIOSCOREA, DOLICHOS, IRIS VERSICOLOR, JUNIPERUS COM., NUX VOM.,PTELEA,TARAXACUM, CARDUUS MAR., CYNARA SCOLYMUS, SOLIDAGO	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-2419-1	openfda.package_ndc
ndc	package	55714-2419-2	openfda.package_ndc
ndc	product	55714-2419	openfda.product_ndc
ndc11	package	55714241902	derived:openfda.package_ndc
ndc11	package	55714241901	derived:openfda.package_ndc
spl id		b4e1c678-878e-07b1-e053-2a95a90a909e	id
spl set id		92ad49e0-2cfe-7d51-e053-2995a90a16f5	set_id
unii		IWY3IWX2G8	openfda.unii
unii		268B43MJ25	openfda.unii
unii		3E271BSI0C	openfda.unii
unii		7E889U5RNN	openfda.unii
unii		269XH13919	openfda.unii
unii		5KQR6FTT0D	openfda.unii
unii		8SKN0B0MIM	openfda.unii
unii		1TH8Q20J0U	openfda.unii
unii		39981FM375	openfda.unii
unii		6L5ZL09795	openfda.unii
unii		U946SH95EE	openfda.unii
unii		3Q034RO3BT	openfda.unii
unii		25B1Y14T8N	openfda.unii
unii		S003A158SB	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		O84B5194RL	openfda.unii
unii		5405K23S50	openfda.unii
unii		X43D4L3DQC	openfda.unii
unii		B71UA545DE	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 SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.

Reported adverse events (FAERS/openFDA)#

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