Aspartame MSG Detox

Product NDC

43742-0421

11-digit product format

437420421

Labeler code

43742

Product ID

43742-0421_3663232e-3e20-42b4-8862-aa8fe9f96a25

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, Methyl Alcohol, Monosodium Glutamate, Phenylalanine

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2014-06-13

Marketing end

2021-08-06

Substance

CHELIDONIUM MAJUS; PHYTOLACCA AMERICANA ROOT; ARNICA MONTANA; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; BISPHENOL A; DEXTROSE; 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