Emvita 7

Product NDC
66343-094
11-digit product format
663430094
Labeler code
66343
Product ID
66343-094_281734b5-b1cc-74de-e063-6394a90a6e3d
Type
HUMAN OTC DRUG
Nonproprietary name
Anacard occ, Glandula sup, Lachesis mutus, Lycopodium, Phosphorus
Dosage form
LIQUID
Route
ORAL
Labeler
RUBIMED AG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-12-21
Substance
ANACARDIUM OCCIDENTALE FRUIT; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; SUS SCROFA ADRENAL GLAND
Active strength
18; 800; 16; 21; 21 [hp_M]/60mL; [hp_C]/60mL; [hp_M]/60mL; [hp_X]/60mL; [hp_X]/60mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Emvita 7
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANACARDIUM OCCIDENTALE FRUIT18 [hp_M]/60mL
SUS SCROFA ADRENAL GLAND800 [hp_C]/60mL
LACHESIS MUTA VENOM16 [hp_M]/60mL
LYCOPODIUM CLAVATUM SPORE21 [hp_X]/60mL
PHOSPHORUS21 [hp_X]/60mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4A10JR4E7EInternal UNII lookup
398IYQ16YVInternal UNII lookup
VSW71SS07IInternal UNII lookup
C88X29Y479Internal UNII lookup
27YLU75U4WInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
45aa87c9-b12d-4eb9-aa2d-1bd800a4ee6cAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66343-094-60Emvita 760 mL in 1 BOTTLELIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66343-094EMVITA 7 (ANACARD OCC, GLANDULA SUP, LACHESIS MUTUS, LYCOPODIUM, PHOSPHORUS) LIQUID [RUBIMED AG]2Current NDC, Legacy NDC, 1 package rows20241201_45aa87c9-b12d-4eb9-aa2d-1bd800a4ee6c.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 7ANACARD OCC, GLANDULA SUP, LACHESIS MUTUS, LYCOPODIUM, PHOSPHORUSRUBIMED AG45aa87c9-b12d-4eb9-aa2d-1bd800a4ee6c2024-10-29WarningsExact identifier
ndc (product): 66343-094

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66343-094-606634300946060 mL in 1 BOTTLE (66343-094-60) 60 ml2022-12-210000-00-00NoNoCurrent