FDA.reportPublic FDA data

Berberis aquifolium

Product NDC
0220-0831
11-digit product format
002200831
Labeler code
0220
Product ID
0220-0831_3bf0f995-f31f-0716-e063-6294a90a1552
Type
HUMAN OTC DRUG
Nonproprietary name
BERBERIS AQUIFOLIUM ROOT BARK
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
BERBERIS AQUIFOLIUM ROOT BARK
Active strength
30 [hp_C]/30[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BERBERIS AQUIFOLIUM ROOT BARK30 [hp_C]/30[hp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
VZJ9F3C3SBInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
6c422b8e-fa29-a5b2-e053-2991aa0a27d8Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0831-412023-11-09C16284748780-1f386c649-f654-0266-e053-dadaa90a7c1aBerberis aquifolium 30C
0220-0831-412023-01-30C16284748780-1f386c649-f654-0266-e053-dadaa90a7c1aBerberis aquifolium 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0831-41Berberis aquifolium30 [hp_C] in 1 TUBEPELLET304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0831BERBERIS AQUIFOLIUM (BERBERIS AQUIFOLIUM ROOT BARK) PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20231110_6c422b8e-fa29-a5b2-e053-2991aa0a27d8.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
Berberis aquifoliumBERBERIS AQUIFOLIUM ROOT BARKBoiron6c422b8e-fa29-a5b2-e053-2991aa0a27d82025-08-09Exact identifier
ndc (product): 0220-0831

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0831-410022008314130 [hp_C] in 1 TUBE (0220-0831-41) 1983-03-030000-00-00NoNoCurrent