FDA.reportPublic FDA data

Bismuthum subnitricum

Product NDC
0220-0859
11-digit product format
002200859
Labeler code
0220
Product ID
0220-0859_07d93bfb-dc2d-65aa-e063-6394a90a3761
Type
HUMAN OTC DRUG
Nonproprietary name
BISMUTH SUBNITRATE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
BISMUTH SUBNITRATE
Active strength
30 [hp_C]/30[hp_C]
Pharmacologic classes
Bismuth [CS], Bismuth [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Bismuthum subnitricum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BISMUTH SUBNITRATE30 [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
H19J064BA5Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
840e9b46-28c5-35d2-e053-2991aa0a4968Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0be8e4ae-4d57-49f3-b3a9-e4728b4e8d15Product name120240313

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0859-412023-10-16C16284748780-1f386c649-eba1-0266-e053-dadaa90a7c1aBismuthum subnitricum 30C
0220-0859-412023-01-30C16284748780-1f386c649-eba1-0266-e053-dadaa90a7c1aBismuthum subnitricum 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0859-41Bismuthum subnitricum30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0859BISMUTHUM SUBNITRICUM (BISMUTH SUBNITRATE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231017_840e9b46-28c5-35d2-e053-2991aa0a4968.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
Bismuthum subnitricumBISMUTH SUBNITRATEBoiron840e9b46-28c5-35d2-e053-2991aa0a49682023-10-16Exact identifier
ndc (product): 0220-0859

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0859-410022008594130 [hp_C] in 1 TUBE (0220-0859-41) 1983-03-030000-00-00NoNoCurrent