FDA.reportPublic FDA data

Baptisia tinctoria

Product NDC
0220-0775
11-digit product format
002200775
Labeler code
0220
Product ID
0220-0775_09ba7935-c8f7-d228-e063-6294a90a1e29
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
30 [hp_C]/30[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 ROOT30 [hp_C]/30[hp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5EF0HWI5WUInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8463bcfa-7155-3b4f-e053-2991aa0a5cb2Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0775-412023-11-09C16284748780-1f386c649-bae3-0266-e053-dadaa90a7c1aBaptisia tinctoria 30C
0220-0775-412023-01-30C16284748780-1f386c649-bae3-0266-e053-dadaa90a7c1aBaptisia tinctoria 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0775-41Baptisia tinctoria30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0775BAPTISIA TINCTORIA (BAPTISIA TINCTORIA ROOT ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231110_8463bcfa-7155-3b4f-e053-2991aa0a5cb2.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Baptisia tinctoriaBAPTISIA TINCTORIA ROOTBoiron8463bcfa-7155-3b4f-e053-2991aa0a5cb22023-11-09Exact identifier
ndc (product): 0220-0775

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0775-410022007754130 [hp_C] in 1 TUBE (0220-0775-41) 1983-03-030000-00-00NoNoCurrent