FDA.reportPublic FDA data

CORALLIUM RUBRUM

Product NDC
60512-6055
11-digit product format
605126055
Labeler code
60512
Product ID
60512-6055_1057b468-8692-456d-a852-e84c23859fd0
Type
HUMAN OTC DRUG
Nonproprietary name
CORALLIUM RUBRUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CORALLIUM RUBRUM EXOSKELETON
Active strength
8 [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
60512-6055-12025-12-29C16284748780-19d75b9d0-7c45-f424-e053-dadaa90a57ce42f17563-9d38-4f78-803d-40e05a177e7c
60512-6055-12020-01-31C16284748780-19d75b9d0-7c45-f424-e053-dadaa90a57ce42f17563-9d38-4f78-803d-40e05a177e7c

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CORALLIUM RUBRUM EXOSKELETONACTIVE INGREDIENT2CA71K0DLECORALLIUM RUBRUM PELLET [HOMEOLAB USA INC.]1
CORALLIUM RUBRUM EXOSKELETONACTIVE MOIETY2CA71K0DLECORALLIUM RUBRUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCORALLIUM RUBRUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554CORALLIUM RUBRUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6055CORALLIUM RUBRUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20140513_42f17563-9d38-4f78-803d-40e05a177e7c.zip