FDA.reportPublic FDA data

Lithium carbonicum

Product NDC
0220-3128
11-digit product format
002203128
Labeler code
0220
Product ID
0220-3128_0a0e6b08-3f35-b3f7-e063-6394a90ae8e3
Type
HUMAN OTC DRUG
Nonproprietary name
LITHIUM CARBONATE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
LITHIUM CARBONATE
Active strength
200 [kp_C]/200[kp_C]
Pharmacologic classes
Mood Stabilizer [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Lithium carbonicum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LITHIUM CARBONATE200 [kp_C]/200[kp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2BMD2GNA4VInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
861df6e6-46cb-632d-e053-2a91aa0ae9a3Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b3053bb1-353b-4a0b-bca5-28fe7228957cProduct name220250124
8ce6e144-236f-b7be-f690-f06e0c8c6bd3Product name220170725
f09af6ee-c6dd-d0ce-77ad-93508bcdacedProduct name420161205

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-3128-412023-11-13C16284748780-1f386c649-c023-0266-e053-dadaa90a7c1aLithium carbonicum 200CK
0220-3128-412023-01-30C16284748780-1f386c649-c023-0266-e053-dadaa90a7c1aLithium carbonicum 200CK

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3128-41Lithium carbonicum200 [kp_C] in 1 TUBEPELLET2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3128LITHIUM CARBONICUM (LITHIUM CARBONATE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231114_861df6e6-46cb-632d-e053-2a91aa0ae9a3.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
Lithium carbonicumLITHIUM CARBONATEBoiron861df6e6-46cb-632d-e053-2a91aa0ae9a32023-11-13Exact identifier
ndc (product): 0220-3128

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-3128-4100220312841200 [kp_C] in 1 TUBE (0220-3128-41) 1983-03-030000-00-00NoNoCurrent