FDA.reportPublic FDA data

PODOPHYLLUM PELTATUM

Product NDC
60512-1038
11-digit product format
605121038
Labeler code
60512
Product ID
60512-1038_5ecb5ce1-ed50-4d14-882c-6f05310a1637
Type
HUMAN OTC DRUG
Nonproprietary name
PODOPHYLLUM PELTATUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
PODOPHYLLUM PELTATUM ROOT
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
60512-1038-12025-12-28C16284748780-19d75b9d0-8428-f424-e053-dadaa90a57ce07c93635-93c1-4edc-8465-c746feceb114
60512-1038-12020-01-31C16284748780-19d75b9d0-8428-f424-e053-dadaa90a57ce07c93635-93c1-4edc-8465-c746feceb114

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PODOPHYLLUM PELTATUM ROOTACTIVE INGREDIENT2S713A4VP3PODOPHYLLUM PELTATUM PELLET [HOMEOLAB USA INC.]1
PODOPHYLLUMACTIVE MOIETY2S713A4VP3PODOPHYLLUM PELTATUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GPODOPHYLLUM PELTATUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554PODOPHYLLUM PELTATUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1038PODOPHYLLUM PELTATUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131029_07c93635-93c1-4edc-8465-c746feceb114.zip