FDA.reportPublic FDA data

APIOLUM

Product NDC
60512-6184
11-digit product format
605126184
Labeler code
60512
Product ID
60512-6184_a7f9defd-737a-4c5b-bc4a-b1a1e13dce1a
Type
HUMAN OTC DRUG
Nonproprietary name
APIOLUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
APIOLE (PARSLEY)
Active strength
3 [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
60512-6184-12025-12-28C16284748780-19d75b9cf-d9eb-f424-e053-dadaa90a57ce6bd1a20e-278b-424e-81f3-35c85612033c
60512-6184-12020-01-31C16284748780-19d75b9cf-d9eb-f424-e053-dadaa90a57ce6bd1a20e-278b-424e-81f3-35c85612033c

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
APIOLE (PARSLEY)ACTIVE INGREDIENTQQ67504PXOAPIOLUM PELLET [HOMEOLAB USA INC.]1
APIOLE (PARSLEY)ACTIVE MOIETYQQ67504PXOAPIOLUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAPIOLUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554APIOLUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6184APIOLUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131030_6bd1a20e-278b-424e-81f3-35c85612033c.zip