FDA.reportPublic FDA data

ALNUS GLUTINOSA

Product NDC
60512-6473
11-digit product format
605126473
Labeler code
60512
Product ID
60512-6473_c159ee04-1389-4ff8-9cd9-e8989fd0ca1f
Type
HUMAN OTC DRUG
Nonproprietary name
ALNUS GLUTINOSA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ALNUS GLUTINOSA BARK
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
60512-6473-12025-12-27C16284748780-19d75b9d0-afed-f424-e053-dadaa90a57ceee4825a2-d2c0-402a-9299-823b7824db68
60512-6473-12020-01-31C16284748780-19d75b9d0-afed-f424-e053-dadaa90a57ceee4825a2-d2c0-402a-9299-823b7824db68

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALNUS GLUTINOSA BARKACTIVE INGREDIENT24A0VB48CAALNUS GLUTINOSA PELLET [HOMEOLAB USA INC.]1
ALNUS GLUTINOSA BARKACTIVE MOIETY24A0VB48CAALNUS GLUTINOSA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GALNUS GLUTINOSA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ALNUS GLUTINOSA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6473ALNUS GLUTINOSA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_ee4825a2-d2c0-402a-9299-823b7824db68.zip