FDA.reportPublic FDA data

ANACARDIUM ORIENTALE

Product NDC
60512-6486
11-digit product format
605126486
Labeler code
60512
Product ID
60512-6486_615c8812-ce9e-4cfa-a54c-9a8c474cb7f6
Type
HUMAN OTC DRUG
Nonproprietary name
ANACARDIUM ORIENTALE
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
SEMECARPUS ANACARDIUM JUICE
Active strength
3 [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
60512-6486-12025-12-28C16284748780-19d75b9d1-0729-f424-e053-dadaa90a57ce947e0303-feeb-4c34-9088-d66ef8e74e10
60512-6486-12020-01-31C16284748780-19d75b9d1-0729-f424-e053-dadaa90a57ce947e0303-feeb-4c34-9088-d66ef8e74e10

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SEMECARPUS ANACARDIUM JUICEACTIVE INGREDIENTY0F0BU8RDUANACARDIUM ORIENTALE PELLET [HOMEOLAB USA INC.]1
SEMECARPUS ANACARDIUM JUICEACTIVE MOIETYY0F0BU8RDUANACARDIUM ORIENTALE PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GANACARDIUM ORIENTALE PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ANACARDIUM ORIENTALE PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6486ANACARDIUM ORIENTALE PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_947e0303-feeb-4c34-9088-d66ef8e74e10.zip