Bellis Perennis

Product NDC
66096-798
11-digit product format
660960798
Labeler code
66096
Product ID
66096-798_d450edda-bf91-13b8-e053-2a95a90a3b6b
Type
HUMAN OTC DRUG
Nonproprietary name
BELLIS PERENNIS
Dosage form
PELLET
Route
ORAL
Labeler
OHM PHARMA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-11-01
Substance
BELLIS PERENNIS
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
Bellis Perennis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BELLIS PERENNIS6 [hp_C]/6[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii2HU33I03UY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66096-798-01Bellis Perennis6 [hp_C] in 1 TUBEPELLET63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-798BELLIS PERENNIS PELLET [OHM PHARMA INC.]3Current NDC, Legacy NDC, 1 package rows20211230_c7afe21a-0c22-4487-97b7-eb100e471cf6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
66096-798-01660960798016 [hp_C] in 1 TUBE (66096-798-01) 2019-11-010000-00-00NoNoCurrent