Anagallis Arvensis

Product NDC
53645-2051
11-digit product format
536452051
Labeler code
53645
Product ID
53645-2051_fe17fb5b-9f4f-d9ed-e053-6394a90a0ec5
Type
HUMAN OTC DRUG
Nonproprietary name
Anagallis Arvensis
Dosage form
GLOBULE
Route
ORAL
Labeler
True Botanica, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2014-02-03
Substance
ANAGALLIS ARVENSIS
Active strength
30 [hp_X]/23g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANAGALLIS ARVENSIS30 [hp_X]/23g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii46883LR90E

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53645-2051-32021-01-31C16284748780-1ba0f9c33-3537-a910-e053-dadaa90a0b85Anagallis Arvensis 30X
53645-2051-32021-01-29C16284748780-1ba0f9c33-3537-a910-e053-dadaa90a0b85Anagallis Arvensis 30X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53645-2051-2Anagallis Arvensis23 g in 1 BOTTLEGLOBULE236

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53645-2051ANAGALLIS ARVENSIS GLOBULE [TRUE BOTANICA, LLC]6Current NDC, Legacy NDC, 1 package rows20230621_6199ad50-408f-4fee-e053-2991aa0aaf5e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53645-2051-25364520510223 g in 1 BOTTLE (53645-2051-2) 23 g2014-02-03NoNoCurrent
53645-2051-35364520510323 g in 1 BOTTLE (53645-2051-3) 23 g2014-02-030000-00-00NoNoCurrent