Gluten Detox

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: Gluten Detox
Generic name: BARLEY (GRAIN), CARBO VEGETABILIS, CINCHONA OFFICINALIS, GLUTEN, GLYPHOSATE, HYDRASTIS CANADENSIS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, NUX VOMICA, OAT (GRAIN), PANCREAS SUIS, PULSATILLA (VULGARIS), RYE (GRAIN), WHEAT (GRAIN)
Manufacturer: Liddell Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 706f2e33-8674-4911-ba0a-4efc935e7739
SPL ID: cc23063d-ac38-4ad9-9479-7504cd915b19
Version: 4
Effective date: 2024-11-04
Source export date: 2026-10-12
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:12:54

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Gluten Detox	openfda.brand_name
generic name		BARLEY (GRAIN), CARBO VEGETABILIS, CINCHONA OFFICINALIS, GLUTEN, GLYPHOSATE, HYDRASTIS CANADENSIS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, NUX VOMICA, OAT (GRAIN), PANCREAS SUIS, PULSATILLA (VULGARIS), RYE (GRAIN), WHEAT (GRAIN)	openfda.generic_name
manufacturer name		Liddell Laboratories, Inc.	openfda.manufacturer_name
ndc	package	50845-0234-2	openfda.package_ndc
ndc	package	50845-0234-1	openfda.package_ndc
ndc	product	50845-0234	openfda.product_ndc
ndc11	package	50845023401	derived:openfda.package_ndc
ndc11	package	50845023402	derived:openfda.package_ndc
spl id		cc23063d-ac38-4ad9-9479-7504cd915b19	id
spl set id		706f2e33-8674-4911-ba0a-4efc935e7739	set_id
unii		2P3VWU3H10	openfda.unii
unii		269XH13919	openfda.unii
unii		8PI54V663Y	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		5PWM7YLI7R	openfda.unii
unii		ZW3Z11D0JV	openfda.unii
unii		S003A158SB	openfda.unii
unii		4632WW1X5A	openfda.unii
unii		0R4AQI398X	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		C88X29Y479	openfda.unii
unii		4J2I0SN84Y	openfda.unii
unii		9Y3J3362RY	openfda.unii
unii		1534K8653J	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: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast feeding, ask a doctor before use. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

Reported adverse events (FAERS/openFDA)#

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