Aspartame/MSG 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: Aspartame/MSG Detox
Generic name: CHELIDONIUM MAJUS, ARNICA MONTANA, PHYTOLACCA DECANDRA, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM, BISPHENOL A (BPA), DEXTROSE, MALTODEXTRIN, SUCRALOSE, ASPARTIC ACID, DIKETOPIPERAZINE, DOPAMINE HYDROCHLORIDE, FORMALINUM, FORMICUM ACIDUM, L-PHENYLALANINE, METHYL ALCOHOL, MONOSODIUM GLUTAMATE
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: a1dc1bf3-db71-4550-a975-4f146fb94005
SPL ID: 634f9781-38c1-438b-8535-1a7ebe40fbb8
Version: 3
Effective date: 2025-03-11
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 07:54:00

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 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Aspartame/MSG Detox	openfda.brand_name
generic name		CHELIDONIUM MAJUS, ARNICA MONTANA, PHYTOLACCA DECANDRA, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM, BISPHENOL A (BPA), DEXTROSE, MALTODEXTRIN, SUCRALOSE, ASPARTIC ACID, DIKETOPIPERAZINE, DOPAMINE HYDROCHLORIDE, FORMALINUM, FORMICUM ACIDUM, L-PHENYLALANINE, METHYL ALCOHOL, MONOSODIUM GLUTAMATE	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1252-1	openfda.package_ndc
ndc	product	43742-1252	openfda.product_ndc
ndc11	package	43742125201	derived:openfda.package_ndc
spl id		634f9781-38c1-438b-8535-1a7ebe40fbb8	id
spl set id		a1dc1bf3-db71-4550-a975-4f146fb94005	set_id
unii		11E6VI8VEG	openfda.unii
unii		0YIW783RG1	openfda.unii
unii		7E889U5RNN	openfda.unii
unii		Y4S76JWI15	openfda.unii
unii		269XH13919	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		411VRN1TV4	openfda.unii
unii		7L3E358N9L	openfda.unii
unii		30KYC7MIAI	openfda.unii
unii		W81N5U6R6U	openfda.unii
unii		MLT3645I99	openfda.unii
unii		47E5O17Y3R	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		96K6UQ3ZD4	openfda.unii
unii		1HG84L3525	openfda.unii
unii		LX22YL083G	openfda.unii
unii		240L69DTV7	openfda.unii
unii		7CVR7L4A2D	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 breastfeeding, 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.