FDA.reportPublic FDA data

ABELMOSCHUS

Product NDC
60512-6435
11-digit product format
605126435
Labeler code
60512
Product ID
60512-6435_45084b0d-210b-4fc5-afa7-2f83fb28924e
Type
HUMAN OTC DRUG
Nonproprietary name
ABELMOSCHUS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-14
Marketing end
0000-00-00
Substance
ABELMOSCHUS MOSCHATUS SEED
Active strength
6 [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
60512-6435-12025-12-28C16284748780-19d75b9cf-da15-f424-e053-dadaa90a57ce534ed9f1-2763-4fd5-8ba9-0cd7e1aa5e5d
60512-6435-12020-01-31C16284748780-19d75b9cf-da15-f424-e053-dadaa90a57ce534ed9f1-2763-4fd5-8ba9-0cd7e1aa5e5d

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ABELMOSCHUS MOSCHATUS SEEDACTIVE INGREDIENTUN2QZ55I88ABELMOSCHUS PELLET [HOMEOLAB USA INC]1
ABELMOSCHUS MOSCHATUS SEEDACTIVE MOIETYUN2QZ55I88ABELMOSCHUS PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GABELMOSCHUS PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554ABELMOSCHUS PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6435ABELMOSCHUS PELLET [HOMEOLAB USA INC]1Legacy NDC20131115_534ed9f1-2763-4fd5-8ba9-0cd7e1aa5e5d.zip