FDA.reportPublic FDA data

ALOE

Product NDC
60512-6475
11-digit product format
605126475
Labeler code
60512
Product ID
60512-6475_464b4639-3bb8-4ccc-80a9-db911108be7e
Type
HUMAN OTC DRUG
Nonproprietary name
ALOE
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-14
Marketing end
0000-00-00
Substance
ALOE VERA LEAF
Active strength
6 [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
60512-6475-12025-12-28C16284748780-19d75b9d0-b5ab-f424-e053-dadaa90a57ce31c2e372-f4df-4fa2-b451-1c1e246be338
60512-6475-12020-01-31C16284748780-19d75b9d0-b5ab-f424-e053-dadaa90a57ce31c2e372-f4df-4fa2-b451-1c1e246be338

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALOE VERA LEAFACTIVE INGREDIENTZY81Z83H0XALOE PELLET [HOMEOLAB USA INC.]1
ALOE VERA LEAFACTIVE MOIETYZY81Z83H0XALOE PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GALOE PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ALOE PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6475ALOE PELLET [HOMEOLAB USA INC.]1Legacy NDC20131115_31c2e372-f4df-4fa2-b451-1c1e246be338.zip