Bellis perennis

Product NDC
0220-0734
11-digit product format
002200734
Labeler code
0220
Product ID
0220-0734_09ba5e8f-735b-2a35-e063-6394a90a98d0
Type
HUMAN OTC DRUG
Nonproprietary name
BELLIS PERENNIS
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
BELLIS PERENNIS
Active strength
1 [hp_M]/[hp_M]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Bellis perennis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BELLIS PERENNIS1 [hp_M]/[hp_M]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii2HU33I03UY

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0734-412023-11-09C16284748780-1f386c649-99fb-0266-e053-dadaa90a7c1aBellis perennis 1M
0220-0734-412023-01-30C16284748780-1f386c649-99fb-0266-e053-dadaa90a7c1aBellis perennis 1M

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0734-41Bellis perennis1 [hp_M] in 1 TUBEPELLET12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0734BELLIS PERENNIS (BELLIS PERENNIS ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231110_850084c3-1dd2-eb8d-e053-2a91aa0a130b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0734-41002200734411 [hp_M] in 1 TUBE (0220-0734-41) 1983-03-030000-00-00NoNoCurrent