Baptisia Tinctoria

Product NDC
66096-794
11-digit product format
660960794
Labeler code
66096
Product ID
66096-794_d450d478-256b-86e2-e053-2995a90a06ab
Type
HUMAN OTC DRUG
Nonproprietary name
BAPTISIA TINCTORIA
Dosage form
PELLET
Route
ORAL
Labeler
OHM PHARMA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-11-01
Substance
BAPTISIA TINCTORIA ROOT
Active strength
6 [hp_C]/6[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Baptisia Tinctoria
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BAPTISIA TINCTORIA ROOT6 [hp_C]/6[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5EF0HWI5WU

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66096-794-01Baptisia Tinctoria6 [hp_C] in 1 TUBEPELLET63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-794BAPTISIA TINCTORIA PELLET [OHM PHARMA INC.]3Current NDC, Legacy NDC, 1 package rows20211230_2c52a2ad-4921-4a6f-a242-e87021d876fb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
66096-794-01660960794016 [hp_C] in 1 TUBE (66096-794-01) 2019-11-010000-00-00NoNoCurrent