Sepia

Product NDC
0220-4662
11-digit product format
002204662
Labeler code
0220
Product ID
0220-4662_0a33c788-2062-5531-e063-6294a90a9598
Type
HUMAN OTC DRUG
Nonproprietary name
SEPIA OFFICINALIS JUICE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
SEPIA OFFICINALIS JUICE
Active strength
30 [hp_X]/30[hp_X]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SEPIA OFFICINALIS JUICE30 [hp_X]/30[hp_X]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiQDL83WN8C2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-4662-412023-11-15C16284748780-1f386c649-df30-0266-e053-dadaa90a7c1aSepia 30X
0220-4662-412023-01-30C16284748780-1f386c649-df30-0266-e053-dadaa90a7c1aSepia 30X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-4662-41Sepia30 [hp_X] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-4662SEPIA (SEPIA OFFICINALIS JUICE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231116_86d2b39f-b7ae-6630-e053-2991aa0a8f90.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-4662-410022046624130 [hp_X] in 1 TUBE (0220-4662-41) 1983-03-030000-00-00NoNoCurrent