FDA.reportPublic FDA data

CETRARIA ISLANDICA

Product NDC
60512-6582
11-digit product format
605126582
Labeler code
60512
Product ID
60512-6582_fdcb1441-b829-4ddf-a5b9-1a51624261ae
Type
HUMAN OTC DRUG
Nonproprietary name
CETRARIA ISLANDICA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CETRARIA ISLANDICA SUBSP. ISLANDICA
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
60512-6582-12025-12-30C16284748780-19d75b9d0-30d9-f424-e053-dadaa90a57ce7b5b9c63-6af9-446e-9fc2-b726b9e352d0
60512-6582-12020-01-31C16284748780-19d75b9d0-30d9-f424-e053-dadaa90a57ce7b5b9c63-6af9-446e-9fc2-b726b9e352d0

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CETRARIA ISLANDICA SUBSP. ISLANDICAACTIVE INGREDIENTBJ7YPN79A1CETRARIA ISLANDICA PELLET [HOMEOLAB USA INC.]1
CETRARIA ISLANDICA SUBSP. ISLANDICAACTIVE MOIETYBJ7YPN79A1CETRARIA ISLANDICA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCETRARIA ISLANDICA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554CETRARIA ISLANDICA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6582CETRARIA ISLANDICA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_7b5b9c63-6af9-446e-9fc2-b726b9e352d0.zip