FDA.reportPublic FDA data

Emvita 5

Product NDC
66343-092
11-digit product format
663430092
Labeler code
66343
Product ID
66343-092_2817dd5d-4be8-2e80-e063-6394a90acfd9
Type
HUMAN OTC DRUG
Nonproprietary name
Bufo rana, Cuprum metallicum, Glandula suprarenalis, Phosphorus, Pulsatilla, Zincum metallicum
Dosage form
LIQUID
Route
ORAL
Labeler
RUBIMED AG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-12-21
Substance
BUFO BUFO CUTANEOUS GLAND; COPPER; PHOSPHORUS; PULSATILLA VULGARIS WHOLE; SUS SCROFA ADRENAL GLAND; ZINC
Active strength
800; 18; 21; 16; 21; 21 [hp_C]/60mL; [hp_M]/60mL; [hp_X]/60mL; [hp_M]/60mL; [hp_X]/60mL; [hp_X]/60mL
Pharmacologic classes
Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Emvita 5
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BUFO BUFO CUTANEOUS GLAND800 [hp_C]/60mL
COPPER18 [hp_M]/60mL
SUS SCROFA ADRENAL GLAND21 [hp_X]/60mL
PHOSPHORUS16 [hp_M]/60mL
PULSATILLA VULGARIS WHOLE21 [hp_X]/60mL
ZINC21 [hp_X]/60mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 6 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
Q59QU6N72QInternal UNII lookup
789U1901C5Internal UNII lookup
398IYQ16YVInternal UNII lookup
27YLU75U4WInternal UNII lookup
I76KB35JEVInternal UNII lookup
J41CSQ7QDSInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
2a141ded-a864-422f-8eb4-69d65fb59c15Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66343-092-60Emvita 560 mL in 1 BOTTLELIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66343-092EMVITA 5 (BUFO RANA, CUPRUM METALLICUM, GLANDULA SUPRARENALIS, PHOSPHORUS, PULSATILLA, ZINCUM METALLICUM) LIQUID [RUBIMED AG]2Current NDC, Legacy NDC, 1 package rows20241201_2a141ded-a864-422f-8eb4-69d65fb59c15.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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Emvita 5BUFO RANA, CUPRUM METALLICUM, GLANDULA SUPRARENALIS, PHOSPHORUS, PULSATILLA, ZINCUM METALLICUMRUBIMED AG2a141ded-a864-422f-8eb4-69d65fb59c152024-10-29WarningsExact identifier
ndc (product): 66343-092

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66343-092-606634300926060 mL in 1 BOTTLE (66343-092-60) 60 ml2022-12-210000-00-00NoNoCurrent