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
HYPERICUM PERFORATUM21 [hp_X]/59mL
SEMECARPUS ANACARDIUM JUICE12 [hp_X]/59mL
SUS SCROFA CEREBRUM200 [hp_C]/59mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU0NQ8555JD, XK4IUX8MNB, Y0F0BU8RDU, 4GB5DQR532

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

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