FDA.reportPublic FDA data

FUCUS VESICULOSUS

Product NDC
60512-6695
11-digit product format
605126695
Labeler code
60512
Product ID
60512-6695_700fa09c-5049-427a-a655-a91b2281a9fd
Type
HUMAN OTC DRUG
Nonproprietary name
FUCUS VESICULOSUS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-18
Marketing end
0000-00-00
Substance
FUCUS VESICULOSUS
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
60512-6695-12025-12-30C16284748780-19d75b9d0-4ff0-f424-e053-dadaa90a57ce8f43f2a9-7038-4f1d-9249-93302f183b94
60512-6695-12020-01-31C16284748780-19d75b9d0-4ff0-f424-e053-dadaa90a57ce8f43f2a9-7038-4f1d-9249-93302f183b94

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FUCUS VESICULOSUSACTIVE INGREDIENT535G2ABX9MFUCUS VESICULOSUS PELLET [HOMEOLAB USA INC.]1
FUCUS VESICULOSUSACTIVE MOIETY535G2ABX9MFUCUS VESICULOSUS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GFUCUS VESICULOSUS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554FUCUS VESICULOSUS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6695FUCUS VESICULOSUS PELLET [HOMEOLAB USA INC.]1Legacy NDC20140513_8f43f2a9-7038-4f1d-9249-93302f183b94.zip