FDA.reportPublic FDA data

ALLIUM CEPA

Product NDC
60512-1002
11-digit product format
605121002
Labeler code
60512
Product ID
60512-1002_19e754b3-7293-49e5-a700-a10b2b22f311
Type
HUMAN OTC DRUG
Nonproprietary name
ALLIUM CEPA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ONION
Active strength
1 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-1002-12025-12-28C16284748780-19d75b9d0-0100-f424-e053-dadaa90a57ce3f9ca4b6-b384-4e2a-a7da-b09cdfb14904
60512-1002-12020-01-31C16284748780-19d75b9d0-0100-f424-e053-dadaa90a57ce3f9ca4b6-b384-4e2a-a7da-b09cdfb14904

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ONIONACTIVE INGREDIENT492225Q21HALLIUM CEPA PELLET [HOMEOLAB USA INC]1
ONIONACTIVE MOIETY492225Q21HALLIUM CEPA PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GALLIUM CEPA PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554ALLIUM CEPA PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1002ALLIUM CEPA PELLET [HOMEOLAB USA INC]1Legacy NDC20111201_3f9ca4b6-b384-4e2a-a7da-b09cdfb14904.zip