FDA.reportPublic FDA data

Xanthoxylum fraxineum

Product NDC
0220-5335
11-digit product format
002205335
Labeler code
0220
Product ID
0220-5335_00edb97e-6152-1534-e063-6294a90ab766
Type
HUMAN OTC DRUG
Nonproprietary name
ZANTHOXYLUM AMERICANUM BARK
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
ZANTHOXYLUM AMERICANUM 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
Xanthoxylum fraxineum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZANTHOXYLUM AMERICANUM 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
A4KL1HMZ7TInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
8143ad9d-7029-fa2f-e053-2a91aa0a33acAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-5335-412023-07-20C16284748780-1f386c649-ebaa-0266-e053-dadaa90a7c1aXanthoxylum fraxineum 30C
0220-5335-412023-01-30C16284748780-1f386c649-ebaa-0266-e053-dadaa90a7c1aXanthoxylum fraxineum 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-5335-41Xanthoxylum fraxineum30 [hp_C] in 1 TUBEPELLET303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-5335XANTHOXYLUM FRAXINEUM (ZANTHOXYLUM AMERICANUM BARK) PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20230721_8143ad9d-7029-fa2f-e053-2a91aa0a33ac.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
Xanthoxylum fraxineumZANTHOXYLUM AMERICANUM BARKBoiron8143ad9d-7029-fa2f-e053-2a91aa0a33ac2023-07-20Exact identifier
ndc (product): 0220-5335

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-5335-410022053354130 [hp_C] in 1 TUBE (0220-5335-41) 1983-03-030000-00-00NoNoCurrent