FDA.reportPublic FDA data

Emvita 16

Product NDC
66343-103
11-digit product format
663430103
Labeler code
66343
Product ID
66343-103_2817453b-92bd-a7d3-e063-6394a90a8d59
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitum napellus, Ambra grisea, Eschscholtzia, Secale, Thymus gland, Zinc met
Dosage form
LIQUID
Route
ORAL
Labeler
RUBIMED AG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-12-23
Substance
ACONITUM NAPELLUS WHOLE; AMBERGRIS; BOS TAURUS THYMUS; CLAVICEPS PURPUREA SCLEROTIUM; ESCHSCHOLZIA CALIFORNICA WHOLE; ZINC
Active strength
800; 18; 21; 21; 16; 21 [hp_C]/60mL; [hp_M]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_M]/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 16
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS WHOLE800 [hp_C]/60mL
AMBERGRIS18 [hp_M]/60mL
BOS TAURUS THYMUS21 [hp_X]/60mL
CLAVICEPS PURPUREA SCLEROTIUM21 [hp_X]/60mL
ESCHSCHOLZIA CALIFORNICA WHOLE16 [hp_M]/60mL
ZINC21 [hp_X]/60mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU0NQ8555JD, XTC0D02P6C, 8XEJ88V2T8, 01G9XEA93N, 9315HN272X, J41CSQ7QDS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66343-103-60Emvita 1660 mL in 1 BOTTLELIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66343-103EMVITA 16 (ACONITUM NAPELLUS, AMBRA GRISEA, ESCHSCHOLTZIA, SECALE, THYMUS GLAND, ZINC MET) LIQUID [RUBIMED AG]2Current NDC, Legacy NDC, 1 package rows20241201_b681ec83-cc7f-4c8e-80a8-0aa0b1cc0759.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66343-103-606634301036060 mL in 1 BOTTLE (66343-103-60) 60 ml2022-12-230000-00-00NoNoCurrent