FDA.reportPublic FDA data

Emvita 18

Product NDC
66343-105
Requested package NDC
66343-105-60
11-digit product format
663430105
Labeler code
66343
Product ID
66343-105_5fa629e1-8c93-e2cf-e063-6394a90afa97
Type
HUMAN OTC DRUG
Nonproprietary name
Agaricus muscarius, Bufo rana, Cuprum met, Thyroidinum, Iodium
Dosage form
LIQUID
Route
ORAL
Labeler
RUBIMED AG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-12-23
Substance
AMANITA MUSCARIA FRUITING BODY; BUFO BUFO CUTANEOUS GLAND; COPPER; SUS SCROFA THYROID; IODINE
Active strength
800; 21; 18; 21; 21 [hp_C]/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
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Emvita 18
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMANITA MUSCARIA FRUITING BODY800 [hp_C]/60mL
BUFO BUFO CUTANEOUS GLAND21 [hp_X]/60mL
COPPER18 [hp_M]/60mL
SUS SCROFA THYROID21 [hp_X]/60mL
IODINE21 [hp_X]/60mL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
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
66343-105-60Emvita 1860 mL in 1 BOTTLELIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66343-105EMVITA 18 (AGARICUS MUSCARIUS, BUFO RANA, CUPRUM MET, THYROIDINUM, IODIUM) LIQUID [RUBIMED AG]2Current NDC, Legacy NDC, 1 package rows20241201_ce1d02fc-8e6d-4893-875f-bb10e7466520.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 18AGARICUS MUSCARIUS, BUFO RANA, CUPRUM MET, THYROIDINUM, IODIUMRUBIMED AGce1d02fc-8e6d-4893-875f-bb10e74665202024-10-29WarningsExact identifier
ndc (package): 66343-105-60
ndc (product): 66343-105
ndc11 (package): 66343010560

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66343-105-606634301056060 mL in 1 BOTTLE (66343-105-60) 60 ml2022-12-230000-00-00NoNoCurrent