FDA.reportPublic FDA data

Lithium Carb

Product NDC
44911-0147
11-digit product format
449110147
Labeler code
44911
Product ID
44911-0147_d87b0a83-30c6-4224-ba49-1ecdf6fb13ea
Type
HUMAN OTC DRUG
Nonproprietary name
Lithium Carbonicum
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-05-12
Substance
LITHIUM CARBONATE
Active strength
12 [hp_X]/mL
Pharmacologic classes
Mood Stabilizer [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LITHIUM CARBONATE12 [hp_X]/mL

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
5fc8a351-c8c6-4a48-a4fc-abda5e8f9a7cAvailable 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
44911-0147-12024-02-27C16284748780-11030e365-6e7d-111a-e063-dadaa90a10e2DRUG FACTS:
44911-0147-12024-01-30C16284748780-11030e365-6e7d-111a-e063-dadaa90a10e2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0147-1Lithium Carb30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LITHIUM CARBONATEACTIVE INGREDIENT2BMD2GNA4VLITHIUM CARB (LITHIUM CARBICUM) LIQUID [ENERGIQUE, INC.]1
LITHIUM CATIONACTIVE MOIETY8H8Z5UER66LITHIUM CARB (LITHIUM CARBICUM) LIQUID [ENERGIQUE, INC.]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MLITHIUM CARB (LITHIUM CARBICUM) LIQUID [ENERGIQUE, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RLITHIUM CARB (LITHIUM CARBICUM) LIQUID [ENERGIQUE, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0147LITHIUM CARB (LITHIUM CARBONICUM) LIQUID [ENERGIQUE, INC.]5Current NDC, Legacy NDC, 1 package rows20240229_5fc8a351-c8c6-4a48-a4fc-abda5e8f9a7c.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 CarbLITHIUM CARBONICUMEnergique, Inc.5fc8a351-c8c6-4a48-a4fc-abda5e8f9a7c2024-02-27WarningsExact identifier
ndc (product): 44911-0147

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0147-14491101470130 mL in 1 BOTTLE, DROPPER (44911-0147-1) 30 ml2015-05-120000-00-00NoNoCurrent