Label: CEREBROMAX (acetylcholine chloride, taurine, adenosinum cyclophosphoricum, cerebrum suis, diencephalon (suis), pineal gland (suis), thalamus opticus (suis), adrenalinum, dopamine hydrochloride, gaba (gamma-aminobutyric acid), norepinephrine (bitartrate), serotonin- hydrochloride, tyramine liquid
- NDC Code(s): 43742-1486-1
- Packager: Deseret Biologicals, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated February 19, 2024
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ACTIVE INGREDIENTS:
Acetylcholine Chloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adenosinum Cyclophosphoricum 8X, Adrenalinum 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Cerebrum Suis 8X, Diencephalon (Suis) 8X, Dopamine Hydrochloride 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, GABA (Gamma-Aminobutyric Acid) 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Norepinephrine (Bitartrate) 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Pineal Gland (Suis) 8X, Serotonin (Hydrochloride) 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Taurine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Thalamus Opticus (Suis) 8X, Tyramine 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.
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PURPOSE:
Acetylcholine Chloride – Memory Problems, Adenosinum Cyclophosphoricum – Emotional Problems, Adrenalinum – Sleep Problems, Cerebrum Suis – Sleep Problems, Diencephalon (Suis) – Memory Problems, Dopamine Hydrochloride – Emotional Problems, GABA (Gamma-Aminobutyric Acid) – Sleep Problems, Norepinephrine (Bitartrate) – Memory Problems, Pineal Gland – Emotional Problems, Serotonin (Hydrochloride) – Sleep Problems, Taurine – Memory Problems, Thalamus Opticus (Suis) – Emotional Problems, Tyramine – Sleep Problems.
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INGREDIENTS AND APPEARANCE
CEREBROMAX
acetylcholine chloride, taurine, adenosinum cyclophosphoricum, cerebrum suis, diencephalon (suis), pineal gland (suis), thalamus opticus (suis), adrenalinum, dopamine hydrochloride, gaba (gamma-aminobutyric acid), norepinephrine (bitartrate), serotonin (hydrochloride), tyramine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-1486 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETYLCHOLINE CHLORIDE (UNII: AF73293C2R) (ACETYLCHOLINE - UNII:N9YNS0M02X) ACETYLCHOLINE CHLORIDE 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 EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH) EPINEPHRINE 8 [hp_X] in 1 mL DOPAMINE HYDROCHLORIDE (UNII: 7L3E358N9L) (DOPAMINE - UNII:VTD58H1Z2X) DOPAMINE HYDROCHLORIDE 8 [hp_X] in 1 mL .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I) (.GAMMA.-AMINOBUTYRIC ACID - UNII:2ACZ6IPC6I) .GAMMA.-AMINOBUTYRIC ACID 8 [hp_X] in 1 mL NOREPINEPHRINE BITARTRATE (UNII: IFY5PE3ZRW) (NOREPINEPHRINE - UNII:X4W3ENH1CV) NOREPINEPHRINE 8 [hp_X] in 1 mL SEROTONIN HYDROCHLORIDE (UNII: GKN429M9VS) (SEROTONIN - UNII:333DO1RDJY) SEROTONIN HYDROCHLORIDE 8 [hp_X] in 1 mL TYRAMINE (UNII: X8ZC7V0OX3) (TYRAMINE - UNII:X8ZC7V0OX3) TYRAMINE 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:43742-1486-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/17/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/17/2019 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-1486) , api manufacture(43742-1486) , label(43742-1486) , pack(43742-1486)
