Baptisia tinctoria

Product NDC
0220-0773
11-digit product format
002200773
Labeler code
0220
Product ID
0220-0773_09ba859c-0875-4ca0-e063-6394a90a14f4
Type
HUMAN OTC DRUG
Nonproprietary name
BAPTISIA TINCTORIA ROOT
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
BAPTISIA TINCTORIA ROOT
Active strength
6 [hp_C]/1
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]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5EF0HWI5WU

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0773-412023-11-09C16284748780-1f386c64a-033b-0266-e053-dadaa90a7c1aBaptisia tinctoria 6C
0220-0773-412023-01-30C16284748780-1f386c64a-033b-0266-e053-dadaa90a7c1aBaptisia tinctoria 6C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0773-41Baptisia tinctoria80 in 1 TUBEPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0773BAPTISIA TINCTORIA (BAPTISIA TINCTORIA ROOT) PELLET [BOIRON]4Current NDC, Legacy NDC, 1 package rows20231110_06251b80-7c4d-11e6-82a9-424c58303031.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0220-0773-410022007734180 PELLET in 1 TUBE (0220-0773-41) 80 pellet1983-03-030000-00-00NoNoCurrent