Pulsatilla

Product NDC
0220-4181
11-digit product format
002204181
Labeler code
0220
Product ID
0220-4181_f2f5a8df-2c3c-12a5-e053-2a95a90a9076
Type
HUMAN OTC DRUG
Nonproprietary name
ANEMONE PULSATILLA
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
ANEMONE PULSATILLA
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
Pulsatilla
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANEMONE PULSATILLA6 [hp_C]/6[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiI76KB35JEV

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-4181-41Pulsatilla6 [hp_C] in 1 TUBEPELLET62

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-4181PULSATILLA (ANEMONE PULSATILLA ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230124_86a80207-b86c-07d7-e053-2a91aa0a043f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-4181-41002204181416 [hp_C] in 1 TUBE (0220-4181-41) 1983-03-030000-00-00NoNoCurrent