Aspartame/MSG Detox

Product NDC

43742-0941

11-digit product format

437420941

Labeler code

43742

Product ID

43742-0941_d2f9e5cc-64aa-4a1c-b60c-60a40cc4888f

Type

HUMAN OTC DRUG

Nonproprietary name

Chelidonium Majus, Phytolacca Decandra, Arnica Montana, 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

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2016-12-27

Marketing end

2023-05-01

Substance

CHELIDONIUM MAJUS; PHYTOLACCA AMERICANA ROOT; ARNICA MONTANA; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; BISPHENOL A; DEXTROSE MONOHYDRATE; MALTODEXTRIN; SUCRALOSE; ASPARTIC ACID; 2,5-PIPERAZINEDIONE; DOPAMINE HYDROCHLORIDE; FORMALDEHYDE; FORMIC ACID; METHYL ALCOHOL; MONOSODIUM GLUTAMATE; PHENYLALANINE

Active strength

3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record