FDA.reportPublic FDA data

CACTUS GRANDIFLORUS

Product NDC
60512-6558
11-digit product format
605126558
Labeler code
60512
Product ID
60512-6558_e64e2a8f-f797-4149-8b82-ca11e3c83650
Type
HUMAN OTC DRUG
Nonproprietary name
CACTUS GRANDIFLORUS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
SELENICEREUS GRANDIFLORUS STEM
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
60512-6558-12025-12-31C16284748780-19d75b9cf-d478-f424-e053-dadaa90a57ce3d21c201-52ee-41a1-8b13-b4fac503f14e
60512-6558-12020-01-31C16284748780-19d75b9cf-d478-f424-e053-dadaa90a57ce3d21c201-52ee-41a1-8b13-b4fac503f14e

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SELENICEREUS GRANDIFLORUS STEMACTIVE INGREDIENT7114SV0MYKCACTUS GRANDIFLORUS PELLET [HOMEOLAB USA INC.]1
SELENICEREUS GRANDIFLORUS STEMACTIVE MOIETY7114SV0MYKCACTUS GRANDIFLORUS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCACTUS GRANDIFLORUS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554CACTUS GRANDIFLORUS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6558CACTUS GRANDIFLORUS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131029_3d21c201-52ee-41a1-8b13-b4fac503f14e.zip