Cerebromax
- Product NDC
- 43742-1269
- 11-digit product format
- 437421269
- Labeler code
- 43742
- Product ID
- 43742-1269_7cc2ef1e-cdb2-41d4-a80d-e922b7bdba57
- 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, Serotonin (Hydrochloride)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-09-19
- Marketing end
- 2023-11-07
- 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; 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-1269-1 | 43742126901 | 30 mL in 1 BOTTLE, DROPPER (43742-1269-1) | 30 ml | 2018-09-19 | 2023-11-07 | No | No | Current |