Cerebromax

Product NDC

43742-1423

11-digit product format

437421423

Labeler code

43742

Product ID

43742-1423_2368f2bf-3741-4a8e-ab57-690e738132db

Type

HUMAN OTC DRUG

Nonproprietary name

Acetylcholine Chloride, Octopamine (Hydrochloride), Taurine, Adenosinum Cyclophosphoricum, Cerebrum Suis, Diencephalon (Suis), Pineal Gland (Suis), Thalamus Opticus (Suis), Adrenalinum, Dopamine Hydrochloride, GABA (Gamma-Aminobutyric Acid), Norepinephrine (Bitartrate), Serotonin (Hydrochloride)

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2019-01-29

Marketing end

2025-07-31

Substance

ACETYLCHOLINE CHLORIDE; OCTOPAMINE HYDROCHLORIDE; TAURINE; ADENOSINE CYCLIC PHOSPHATE; SUS SCROFA CEREBRUM; SUS SCROFA DIENCEPHALON; SUS SCROFA PINEAL GLAND; SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS; EPINEPHRINE; DOPAMINE HYDROCHLORIDE; .GAMMA.-AMINOBUTYRIC ACID; NOREPINEPHRINE BITARTRATE; SEROTONIN HYDROCHLORIDE

Active strength

6 [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