FDA.reportPublic FDA data

ALLIUM SATIVUM

Product NDC
60512-6472
11-digit product format
605126472
Labeler code
60512
Product ID
60512-6472_1e03e993-b0ac-47d3-8244-f879648c9c1c
Type
HUMAN OTC DRUG
Nonproprietary name
ALLIUM SATIVUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ALLIUM SATIVUM 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
60512-6472-12025-12-28C16284748780-19d75b9d0-2abb-f424-e053-dadaa90a57ce8146c3a3-3270-448b-87a6-76371eeb9349
60512-6472-12020-01-31C16284748780-19d75b9d0-2abb-f424-e053-dadaa90a57ce8146c3a3-3270-448b-87a6-76371eeb9349

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALLIUM SATIVUM WHOLEACTIVE INGREDIENTIIF21WT8O3ALLIUM SATIVUM PELLET [HOMEOLAB USA INC.]1
ALLIUM SATIVUM WHOLEACTIVE MOIETYIIF21WT8O3ALLIUM SATIVUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GALLIUM SATIVUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ALLIUM SATIVUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6472ALLIUM SATIVUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_8146c3a3-3270-448b-87a6-76371eeb9349.zip