Anxiovita

Product NDC
66343-082
11-digit product format
663430082
Labeler code
66343
Product ID
66343-082_2816f87f-0405-eba7-e063-6394a90ab393
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitum napellus, Anacardium orientale, Cerebrum, Hypericum perforatum
Dosage form
LIQUID
Route
ORAL
Labeler
RUBIMED AG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-11-28
Substance
ACONITUM NAPELLUS; HYPERICUM PERFORATUM; SEMECARPUS ANACARDIUM JUICE; SUS SCROFA CEREBRUM
Active strength
18; 21; 12; 200 [hp_M]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_C]/59mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS18 [hp_M]/59mL
SEMECARPUS ANACARDIUM JUICE21 [hp_X]/59mL
SUS SCROFA CEREBRUM12 [hp_X]/59mL
HYPERICUM PERFORATUM200 [hp_C]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
U0NQ8555JDInternal UNII lookup
Y0F0BU8RDUInternal UNII lookup
4GB5DQR532Internal UNII lookup
XK4IUX8MNBInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
258c677b-1a0a-4315-ba0c-4d9892f0534dAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66343-082-60Anxiovita59 mL in 1 BOTTLELIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66343-082ANXIOVITA (ACONITUM NAPELLUS, ANACARDIUM ORIENTALE, CEREBRUM, HYPERICUM PERFORATUM) LIQUID [RUBIMED AG]2Current NDC, Legacy NDC, 1 package rows20241201_258c677b-1a0a-4315-ba0c-4d9892f0534d.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
AnxiovitaACONITUM NAPELLUS, ANACARDIUM ORIENTALE, CEREBRUM, HYPERICUM PERFORATUMRUBIMED AG258c677b-1a0a-4315-ba0c-4d9892f0534d2024-10-29WarningsExact identifier
ndc (product): 66343-082

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66343-082-606634300826059 mL in 1 BOTTLE (66343-082-60) 59 ml2022-11-280000-00-00NoNoCurrent