FDA.reportPublic FDA data

ALTHAEA OFFICINALIS

Product NDC
60512-6478
11-digit product format
605126478
Labeler code
60512
Product ID
60512-6478_a535cc62-d0ff-4ea7-ab1a-5748218bbacc
Type
HUMAN OTC DRUG
Nonproprietary name
ALTHAEA OFFICINALIS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ALTHAEA OFFICINALIS ROOT
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
60512-6478-12025-12-28C16284748780-19d75b9cf-ffef-f424-e053-dadaa90a57ce9f4144fd-db66-44ab-a61b-094773a3ea68
60512-6478-12020-01-31C16284748780-19d75b9cf-ffef-f424-e053-dadaa90a57ce9f4144fd-db66-44ab-a61b-094773a3ea68

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALTHAEA OFFICINALIS ROOTACTIVE INGREDIENTTRW2FUF47HALTHAEA OFFICINALIS PELLET [HOMEOLAB USA INC.]1
ALTHAEA OFFICINALIS ROOTACTIVE MOIETYTRW2FUF47HALTHAEA OFFICINALIS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GALTHAEA OFFICINALIS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ALTHAEA OFFICINALIS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6478ALTHAEA OFFICINALIS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_9f4144fd-db66-44ab-a61b-094773a3ea68.zip