FDA.reportPublic FDA data

SEPIA

Product NDC
60512-1043
11-digit product format
605121043
Labeler code
60512
Product ID
60512-1043_60678b2c-eb4e-4ae1-b028-00d0a22ebc98
Type
HUMAN OTC DRUG
Nonproprietary name
SEPIA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
SEPIA OFFICINALIS JUICE
Active strength
1 [hp_X]/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-1043-12025-12-30C16284748780-19d75b9d0-576a-f424-e053-dadaa90a57ce09f8dd8c-3b52-494f-b200-026d61ef613d
60512-1043-12020-01-31C16284748780-19d75b9d0-576a-f424-e053-dadaa90a57ce09f8dd8c-3b52-494f-b200-026d61ef613d

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SEPIA OFFICINALIS JUICEACTIVE INGREDIENTQDL83WN8C2SEPIA PELLET [HOMEOLAB USA INC.]1
SEPIA OFFICINALIS JUICEACTIVE MOIETYQDL83WN8C2SEPIA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GSEPIA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554SEPIA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1043SEPIA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131029_09f8dd8c-3b52-494f-b200-026d61ef613d.zip