FDA.reportPublic FDA data

EUCALYPTUS GLOBULUS

Product NDC
60512-6669
11-digit product format
605126669
Labeler code
60512
Product ID
60512-6669_80b01d6e-6ad8-4f8e-82dd-600f50b117fb
Type
HUMAN OTC DRUG
Nonproprietary name
EUCALYPTUS GLOBULUS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-18
Marketing end
0000-00-00
Substance
EUCALYPTUS GLOBULUS LEAF
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
60512-6669-12025-12-30C16284748780-19d75b9d0-5e5d-f424-e053-dadaa90a57ce06f65d13-c8f1-4408-aa8d-ab965f727ed7
60512-6669-12020-01-31C16284748780-19d75b9d0-5e5d-f424-e053-dadaa90a57ce06f65d13-c8f1-4408-aa8d-ab965f727ed7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EUCALYPTUS GLOBULUS LEAFACTIVE INGREDIENTS546YLW6E6EUCALYPTUS GLOBULUS PELLET [HOMEOLAB USA INC.]1
EUCALYPTUS GLOBULUS LEAFACTIVE MOIETYS546YLW6E6EUCALYPTUS GLOBULUS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GEUCALYPTUS GLOBULUS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554EUCALYPTUS GLOBULUS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6669EUCALYPTUS GLOBULUS PELLET [HOMEOLAB USA INC.]1Legacy NDC20140514_06f65d13-c8f1-4408-aa8d-ab965f727ed7.zip