FDA.reportPublic FDA data

Emvita 22

Product NDC
66343-109
11-digit product format
663430109
Labeler code
66343
Product ID
66343-109_2817773c-3799-efaf-e063-6394a90a7db6
Type
HUMAN OTC DRUG
Nonproprietary name
Ambra grisea, Anacard occ, Chamomilla, Crotalus horridus, Hypophysis, Iodium, Phosphorus
Dosage form
LIQUID
Route
ORAL
Labeler
RUBIMED AG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-12-23
Substance
AMBERGRIS; ANACARDIUM OCCIDENTALE FRUIT; CROTALUS HORRIDUS HORRIDUS VENOM; IODINE; MATRICARIA CHAMOMILLA WHOLE; PHOSPHORUS; SUS SCROFA PITUITARY GLAND
Active strength
21; 18; 21; 16; 800; 21; 21 [hp_X]/60mL; [hp_M]/60mL; [hp_X]/60mL; [hp_M]/60mL; [hp_C]/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 22
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMBERGRIS21 [hp_X]/60mL
ANACARDIUM OCCIDENTALE FRUIT18 [hp_M]/60mL
MATRICARIA CHAMOMILLA WHOLE21 [hp_X]/60mL
CROTALUS HORRIDUS HORRIDUS VENOM16 [hp_M]/60mL
SUS SCROFA PITUITARY GLAND800 [hp_C]/60mL
IODINE21 [hp_X]/60mL
PHOSPHORUS21 [hp_X]/60mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
XTC0D02P6CInternal UNII lookup
4A10JR4E7EInternal UNII lookup
G0R4UBI2ZZInternal UNII lookup
YHA2XLJ956Internal UNII lookup
L0PFEMQ1DTInternal UNII lookup
9679TC07X4Internal 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
d0dd7187-4657-4dca-9624-065c4ed0fa4cAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66343-109-60Emvita 2260 mL in 1 BOTTLELIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66343-109EMVITA 22 (AMBRA GRISEA, ANACARD OCC, CHAMOMILLA, CROTALUS HORRIDUS, HYPOPHYSIS, IODIUM, PHOSPHORUS) LIQUID [RUBIMED AG]2Current NDC, Legacy NDC, 1 package rows20241201_d0dd7187-4657-4dca-9624-065c4ed0fa4c.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 22AMBRA GRISEA, ANACARD OCC, CHAMOMILLA, CROTALUS HORRIDUS, HYPOPHYSIS, IODIUM, PHOSPHORUSRUBIMED AGd0dd7187-4657-4dca-9624-065c4ed0fa4c2024-11-29WarningsExact identifier
ndc (product): 66343-109

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66343-109-606634301096060 mL in 1 BOTTLE (66343-109-60) 60 ml2022-12-230000-00-00NoNoCurrent