CEREBROMAX (acetylcholine chloride, adrenalinum, dopamine hydrochloride, gaba, norepinephrine, octopamine, serotonin- hydrochloride, taurine, liquid

Cerebromax by

Drug Labeling and Warnings

Cerebromax by is a Homeopathic medication manufactured, distributed, or labeled by Deseret Biologicals, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Acetylcholine Chloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adrenalinum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Dopamine Hydrochloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Gaba 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Norepinephrine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Octopamine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Serotonin (Hydrochloride) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Taurine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adenosinum Cyclophoricum 8X, Cerebrum (Suis) 8X, Diencephalon 8X, Pineal Gland (Suis) 8X, Thalamus Opticus (Suis) 8X.

INDICATIONS:

For the temporary relief of symptoms relating to sleep, emotional, nervous or memory disorders.

WARNINGS:

​Keep out of reach of children.​ In case of overdose, contact a physician or Poison Control Center right away.

​If pregnant or breast-feeding, ​ask a health professional before use.

Tamper seal: "Sealed for Your protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

​Keep out of reach of children.​ In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

3-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

For the temporary relief of symptoms relating to sleep, emotional, nervous, or memory disorders.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070   www.desbio.com

PACKAGE DISPLAY LABEL:

DESBIO

NDC: 43742-0343-1

HOMEOPATHIC

​CEREBROMAX

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

CEREBROMAX 
acetylcholine chloride, adrenalinum, dopamine hydrochloride, gaba, norepinephrine, octopamine, serotonin (hydrochloride), taurine, liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43742-0343
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETYLCHOLINE CHLORIDE (UNII: AF73293C2R) (ACETYLCHOLINE - UNII:N9YNS0M02X)	ACETYLCHOLINE	6 [hp_X]  in 1 mL
EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH)	EPINEPHRINE	6 [hp_X]  in 1 mL
DOPAMINE HYDROCHLORIDE (UNII: 7L3E358N9L) (DOPAMINE - UNII:VTD58H1Z2X)	DOPAMINE HYDROCHLORIDE	6 [hp_X]  in 1 mL
.GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I) (.GAMMA.-AMINOBUTYRIC ACID - UNII:2ACZ6IPC6I)	.GAMMA.-AMINOBUTYRIC ACID	6 [hp_X]  in 1 mL
NOREPINEPHRINE (UNII: X4W3ENH1CV) (NOREPINEPHRINE - UNII:X4W3ENH1CV)	NOREPINEPHRINE	6 [hp_X]  in 1 mL
OCTOPAMINE (UNII: 14O50WS8JD) (OCTOPAMINE - UNII:14O50WS8JD)	OCTOPAMINE	6 [hp_X]  in 1 mL
SEROTONIN HYDROCHLORIDE (UNII: GKN429M9VS) (SEROTONIN - UNII:333DO1RDJY)	SEROTONIN HYDROCHLORIDE	6 [hp_X]  in 1 mL
TAURINE (UNII: 1EQV5MLY3D) (TAURINE - UNII:1EQV5MLY3D)	TAURINE	6 [hp_X]  in 1 mL
ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N) (ADENOSINE CYCLIC PHOSPHATE - UNII:E0399OZS9N)	ADENOSINE CYCLIC PHOSPHATE	8 [hp_X]  in 1 mL
SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (SUS SCROFA CEREBRUM - UNII:4GB5DQR532)	SUS SCROFA CEREBRUM	8 [hp_X]  in 1 mL
SUS SCROFA DIENCEPHALON (UNII: 23PJ4252VL) (SUS SCROFA DIENCEPHALON - UNII:23PJ4252VL)	SUS SCROFA DIENCEPHALON	8 [hp_X]  in 1 mL
SUS SCROFA PINEAL GLAND (UNII: 050QZ2EDK7) (SUS SCROFA PINEAL GLAND - UNII:050QZ2EDK7)	SUS SCROFA PINEAL GLAND	8 [hp_X]  in 1 mL
SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS (UNII: P146I3107T) (SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS - UNII:P146I3107T)	SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS	8 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43742-0343-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	09/04/2013	09/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/04/2013	09/02/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-0343) , api manufacture(43742-0343) , label(43742-0343) , pack(43742-0343)