Melissa officinalis

Product NDC
0220-3339
11-digit product format
002203339
Labeler code
0220
Product ID
0220-3339_2356b15c-4004-3c38-e063-6394a90a0039
Type
HUMAN OTC DRUG
Nonproprietary name
MELISSA OFFICINALIS
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
MELISSA OFFICINALIS
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
Melissa officinalis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MELISSA OFFICINALIS30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiYF70189L0N

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-3339-412023-11-14C16284748780-1f386c649-e781-0266-e053-dadaa90a7c1aMelissa officinalis 30C
0220-3339-412023-01-30C16284748780-1f386c649-e781-0266-e053-dadaa90a7c1aMelissa officinalis 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3339-41Melissa officinalis30 [hp_C] in 1 TUBEPELLET305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3339MELISSA OFFICINALIS PELLET [BOIRON]5Current NDC, Legacy NDC, 1 package rows20241001_7d79baea-28c3-4d41-e053-2991aa0a5269.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-3339-410022033394130 [hp_C] in 1 TUBE (0220-3339-41) 1983-03-030000-00-00NoNoCurrent