Neurobalance Pro
- Product NDC
- 50181-0070
- 11-digit product format
- 501810070
- Labeler code
- 50181
- Product ID
- 50181-0070_5d8e5108-7d03-4953-b79d-87075365df6d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GABA (Gamma-Aminobutyric Acid), L-Glutamic Acid, Norepinephrine (Bitartrate), Acetylcholine Chloride, L-Dopa, Serotonin (Hydrochloride), Thyroidinum (Suis), Adrenalinum, Baryta Carbonica, Calcarea Carbonica, Anacardium Orientale, Adrenocorticotrophin, Stramonium
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- The Wellness Center for Reseach and Education, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2019-11-19
- Marketing end
- 0000-00-00
- Substance
- .GAMMA.-AMINOBUTYRIC ACID; GLUTAMIC ACID; NOREPINEPHRINE BITARTRATE; ACETYLCHOLINE CHLORIDE; LEVODOPA; SEROTONIN HYDROCHLORIDE; THYROID, PORCINE; EPINEPHRINE; BARIUM CARBONATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SEMECARPUS ANACARDIUM JUICE; CORTICOTROPIN; DATURA STRAMONIUM
- 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_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50181-0070 | NEUROBALANCE PRO (GABA (GAMMA-AMINOBUTYRIC ACID), L-GLUTAMIC ACID, NOREPINEPHRINE (BITARTRATE), ACETYLCHOLINE CHLORIDE, L-DOPA, SEROTONIN (HYDROCHLORIDE), THYROIDINUM (SUIS), ADRENALINUM, BARYTA CARBONICA, CALCAREA CARBONICA, ANACARDIUM ORIENTALE, ADRENOCORTICOTROPHIN, STRAMONIUM) LIQUID [THE WELLNESS CENTER FOR RESEACH AND EDUCATION, INC.] | 1 | Legacy NDC | 20191224_a37237ed-6465-4623-974d-4f9e22d1e8e9.zip |