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
LACHESIS MUTA VENOM800 [hp_C]/60mL
LYCOPODIUM CLAVATUM SPORE16 [hp_M]/60mL
PHOSPHORUS21 [hp_X]/60mL
SUS SCROFA ADRENAL GLAND21 [hp_X]/60mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4A10JR4E7E, VSW71SS07I, C88X29Y479, 27YLU75U4W, 398IYQ16YV

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

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