FDA.reportPublic FDA data

Paeonia officinalis

Product NDC
0220-3900
11-digit product format
002203900
Labeler code
0220
Product ID
0220-3900_0a0b34ba-2f56-27a4-e063-6394a90a0777
Type
HUMAN OTC DRUG
Nonproprietary name
PAEONIA OFFICINALIS ROOT
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
PAEONIA OFFICINALIS ROOT
Active strength
6 [hp_C]/6[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
Paeonia officinalis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PAEONIA OFFICINALIS ROOT6 [hp_C]/6[hp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8R564U2E1PInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
7f72441a-dfb4-1e5a-e053-2a91aa0a39dbAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-3900-412023-11-13C16284748780-1f386c64a-351c-0266-e053-dadaa90a7c1aPaeonia officinalis 6C
0220-3900-412023-01-30C16284748780-1f386c64a-351c-0266-e053-dadaa90a7c1aPaeonia officinalis 6C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3900-41Paeonia officinalis6 [hp_C] in 1 TUBEPELLET63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3900PAEONIA OFFICINALIS (PAEONIA OFFICINALIS ROOT) PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20231114_7f72441a-dfb4-1e5a-e053-2a91aa0a39db.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
Paeonia officinalisPAEONIA OFFICINALIS ROOTBoiron7f72441a-dfb4-1e5a-e053-2a91aa0a39db2023-11-13Exact identifier
ndc (product): 0220-3900

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-3900-41002203900416 [hp_C] in 1 TUBE (0220-3900-41) 1983-03-030000-00-00NoNoCurrent