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 Identifiers#

Field, Values table
FieldValues
UniiH19J064BA5

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

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