FDA.reportPublic FDA data

COCCUS CACTI

Product NDC
60512-7120
11-digit product format
605127120
Labeler code
60512
Product ID
60512-7120_f72d8665-37bd-4543-a919-23b6556c5057
Type
HUMAN OTC DRUG
Nonproprietary name
COCCUS CACTI
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
DACTYLOPIUS COCCUS WHOLE
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
60512-7120-12025-12-29C16284748780-19d75b9d0-b5c9-f424-e053-dadaa90a57ce684e8aa4-96eb-4a6e-9f64-405312a2b29b
60512-7120-12020-01-31C16284748780-19d75b9d0-b5c9-f424-e053-dadaa90a57ce684e8aa4-96eb-4a6e-9f64-405312a2b29b

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DACTYLOPIUS COCCUS WHOLEACTIVE INGREDIENTX0ZL41304TCOCCUS CACTI PELLET [HOMEOLAB USA INC.]1
DACTYLOPIUS COCCUS WHOLEACTIVE MOIETYX0ZL41304TCOCCUS CACTI PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCOCCUS CACTI PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554COCCUS CACTI PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-7120COCCUS CACTI PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_684e8aa4-96eb-4a6e-9f64-405312a2b29b.zip