Neurovita

Product NDC: 66343-117
Requested package NDC: 66343-117-60
11-digit product format: 663430117
Labeler code: 66343
Product ID: 66343-117_4a1b9d0b-2a0c-d566-e063-6294a90afc0a
Type: HUMAN OTC DRUG
Nonproprietary name: Ambra grisea, Cerebrum, Cinchona, Cuprum acet, Melissa, Phosphorus
Dosage form: LIQUID
Route: ORAL
Labeler: RUBIMED AG
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2022-12-27
Substance: AMBERGRIS; SUS SCROFA CEREBRUM; CINCHONA OFFICINALIS BARK; CUPRIC ACETATE; MELISSA OFFICINALIS WHOLE; PHOSPHORUS
Active strength: 21; 21; 50; 200; 4; 12 [hp_X]/60mL; [hp_X]/60mL; [hp_C]/60mL; [hp_C]/60mL; [hp_X]/60mL; [hp_M]/60mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Neurovita
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
AMBERGRIS	21 [hp_X]/60mL
SUS SCROFA CEREBRUM	21 [hp_X]/60mL
CINCHONA OFFICINALIS BARK	50 [hp_C]/60mL
CUPRIC ACETATE	200 [hp_C]/60mL
MELISSA OFFICINALIS WHOLE	4 [hp_X]/60mL
PHOSPHORUS	12 [hp_M]/60mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 6 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
XTC0D02P6C	Internal UNII lookup
4GB5DQR532	Internal UNII lookup
S003A158SB	Internal UNII lookup
39M11XPH03	Internal UNII lookup
YF70189L0N	Internal UNII lookup
27YLU75U4W	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
333b9c94-8457-47b0-8089-c21268b85b92	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
66343-117-60	Neurovita	60 mL in 1 BOTTLE	LIQUID	60		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66343-117	GEOVITA (AMBRA GRISEA, CEREBRUM, CINCHONA, CUPRUM ACET, MELISSA, PHOSPHORUS) LIQUID [RUBIMED AG]	2	Current NDC, Legacy NDC, 1 package rows	20241201_333b9c94-8457-47b0-8089-c21268b85b92.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Neurovita	AMBRA GRISEA, CEREBRUM, CINCHONA, CUPRUM ACET, MELISSA, PHOSPHORUS	RUBIMED AG	333b9c94-8457-47b0-8089-c21268b85b92	2026-02-05	Warnings	Exact identifier ndc (package): 66343-117-60 ndc (product): 66343-117 ndc11 (package): 66343011760

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
XTC0D02P6C	AMBERGRIS	8038-65-1	AMBERGRIS
4GB5DQR532	SUS SCROFA CEREBRUM		SUS SCROFA CEREBRUM
S003A158SB	CINCHONA OFFICINALIS BARK		CINCHONA OFFICINALIS BARK
39M11XPH03	CUPRIC ACETATE	142-71-2	CUPRIC ACETATE
27YLU75U4W	PHOSPHORUS	7723-14-0	PHOSPHORUS

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
66343-117-60	66343011760	60 mL in 1 BOTTLE (66343-117-60)	60 ml	2022-12-27	0000-00-00	No	No	Current