FDA.reportPublic FDA data

DROSERA ROTUNDIFOLIA

Product NDC
60512-1015
11-digit product format
605121015
Labeler code
60512
Product ID
60512-1015_7baaa926-234f-488a-983e-e11c8758d6b8
Type
HUMAN OTC DRUG
Nonproprietary name
DROSERA ROTUNDIFOLIA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-18
Marketing end
0000-00-00
Substance
DROSERA ROTUNDIFOLIA
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
60512-1015-12025-12-30C16284748780-19d75b9d0-ffa6-f424-e053-dadaa90a57ceccf77422-59cf-4b1b-995c-92a2f8d30acc
60512-1015-12020-01-31C16284748780-19d75b9d0-ffa6-f424-e053-dadaa90a57ceccf77422-59cf-4b1b-995c-92a2f8d30acc

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DROSERA ROTUNDIFOLIAACTIVE INGREDIENTQR44N9XPJQDROSERA ROTUNDIFOLIA PELLET [HOMEOLAB USA INC.]1
DROSERA ROTUNDIFOLIAACTIVE MOIETYQR44N9XPJQDROSERA ROTUNDIFOLIA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GDROSERA ROTUNDIFOLIA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554DROSERA ROTUNDIFOLIA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1015DROSERA ROTUNDIFOLIA PELLET [HOMEOLAB USA INC.]1Legacy NDC20140424_ccf77422-59cf-4b1b-995c-92a2f8d30acc.zip