Detox III

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: Detox III
Generic name: DULCAMARA, ECHINACEA (ANGUSTIFOLIA), AESCULUS HIPPOCASTANUM, ANTIMONIUM TARTARICUM, ASCORBICUM ACIDUM, COCCUS CACTI, GALIUM APARINE, GENTIANA LUTEA, GERANIUM ROBERTIANUM, PULSATILLA (PRATENSIS), SARCOLACTICUM ACIDUM, CONIUM MACULATUM, LYMPH NODE (SUIS), SULPHUR, GLANDULA SUPRARENALIS SUIS, L-PHENYLALANINE, CALCAREA PHOSPHORICA, FERRUM PHOSPHORICUM, HEPAR SUIS, HYPOTHALAMUS SUIS, SPLEEN (SUIS), CORTISONE ACETICUM, MERCURIUS SOLUBILIS, BARYTA CARBONICA, GLYPHOSATE, FUNICULUS UMBILICALIS SUIS,TONSIL (SUIS),
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 6f2136ce-4763-4ebd-a9fc-cbbae1f7ce0b
SPL ID: 2ed94953-a1bb-4688-ad02-c956ef2fe32f
Version: 6
Effective date: 2024-02-19
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:29

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 · 44 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Detox III	openfda.brand_name
generic name		DULCAMARA, ECHINACEA (ANGUSTIFOLIA), AESCULUS HIPPOCASTANUM, ANTIMONIUM TARTARICUM, ASCORBICUM ACIDUM, COCCUS CACTI, GALIUM APARINE, GENTIANA LUTEA, GERANIUM ROBERTIANUM, PULSATILLA (PRATENSIS), SARCOLACTICUM ACIDUM, CONIUM MACULATUM, LYMPH NODE (SUIS), SULPHUR, GLANDULA SUPRARENALIS SUIS, L-PHENYLALANINE, CALCAREA PHOSPHORICA, FERRUM PHOSPHORICUM, HEPAR SUIS, HYPOTHALAMUS SUIS, SPLEEN (SUIS), CORTISONE ACETICUM, MERCURIUS SOLUBILIS, BARYTA CARBONICA, GLYPHOSATE, FUNICULUS UMBILICALIS SUIS,TONSIL (SUIS),	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1970-1	openfda.package_ndc
ndc	product	43742-1970	openfda.product_ndc
ndc11	package	43742197001	derived:openfda.package_ndc
spl id		2ed94953-a1bb-4688-ad02-c956ef2fe32f	id
spl set id		6f2136ce-4763-4ebd-a9fc-cbbae1f7ce0b	set_id
unii		SBV4XY874G	openfda.unii
unii		KPS1B1162N	openfda.unii
unii		324Y4038G2	openfda.unii
unii		VP2CN2G7Y8	openfda.unii
unii		LZB7TFX1LT	openfda.unii
unii		883WKN7W8X	openfda.unii
unii		Q28R5GF371	openfda.unii
unii		4R7X1O2820	openfda.unii
unii		S72O3284MS	openfda.unii
unii		6P669D8HQ8	openfda.unii
unii		TB08NIC03W	openfda.unii
unii		91D9GV0Z28	openfda.unii
unii		3C18L6RJAZ	openfda.unii
unii		DL6OZ476V3	openfda.unii
unii		33A7VYU29L	openfda.unii
unii		9679TC07X4	openfda.unii
unii		F9S9FFU82N	openfda.unii
unii		RGL5YE86CZ	openfda.unii
unii		R5I1HK0UBL	openfda.unii
unii		PQ6CK8PD0R	openfda.unii
unii		06LU7C9H1V	openfda.unii
unii		91GQH8I5F7	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		92AMN5J79Y	openfda.unii
unii		Y3V16D4PV4	openfda.unii
unii		MLT3645I99	openfda.unii
unii		8E272251DI	openfda.unii
unii		47E5O17Y3R	openfda.unii
unii		398IYQ16YV	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		4632WW1X5A	openfda.unii
unii		118OYG6W3H	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 professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

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