FDA.reportPublic FDA data

Melilotus officinalis

Product NDC
0220-3335
11-digit product format
002203335
Labeler code
0220
Product ID
0220-3335_0a1f3256-dc5d-91b7-e063-6394a90a0de4
Type
HUMAN OTC DRUG
Nonproprietary name
MELILOTUS OFFICINALIS TOP
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
MELILOTUS OFFICINALIS TOP
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
Melilotus officinalis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MELILOTUS OFFICINALIS TOP6 [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
GM6P02J2DXInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
7d792fea-6c10-0994-e053-2a91aa0a20c1Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-3335-412023-11-14C16284748780-1f386c649-9933-0266-e053-dadaa90a7c1aMelilotus officinalis 6C
0220-3335-412023-01-30C16284748780-1f386c649-9933-0266-e053-dadaa90a7c1aMelilotus officinalis 6C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3335-41Melilotus officinalis6 [hp_C] in 1 TUBEPELLET63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3335MELILOTUS OFFICINALIS (MELILOTUS OFFICINALIS TOP) PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20231115_7d792fea-6c10-0994-e053-2a91aa0a20c1.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
Melilotus officinalisMELILOTUS OFFICINALIS TOPBoiron7d792fea-6c10-0994-e053-2a91aa0a20c12023-11-14Exact identifier
ndc (product): 0220-3335

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-3335-41002203335416 [hp_C] in 1 TUBE (0220-3335-41) 1983-03-030000-00-00NoNoCurrent