FDA.reportPublic FDA data

BAPTISIA TINCTORIA

Product NDC
60512-6537
11-digit product format
605126537
Labeler code
60512
Product ID
60512-6537_6f55f71e-9921-4d01-9213-28eec3fdb6a0
Type
HUMAN OTC DRUG
Nonproprietary name
BAPTISIA TINCTORIA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
BAPTISIA TINCTORIA 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
60512-6537-12025-12-29C16284748780-19d75b9cf-da1e-f424-e053-dadaa90a57ceb8810834-414a-45d8-9ec2-4123ee1b44e7
60512-6537-12020-01-31C16284748780-19d75b9cf-da1e-f424-e053-dadaa90a57ceb8810834-414a-45d8-9ec2-4123ee1b44e7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BAPTISIA TINCTORIA ROOTACTIVE INGREDIENT5EF0HWI5WUBAPTISIA TINCTORIA PELLET [HOMEOLAB USA INC.]1
BAPTISIA TINCTORIA ROOTACTIVE MOIETY5EF0HWI5WUBAPTISIA TINCTORIA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GBAPTISIA TINCTORIA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554BAPTISIA TINCTORIA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6537BAPTISIA TINCTORIA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_b8810834-414a-45d8-9ec2-4123ee1b44e7.zip