FDA.reportPublic FDA data

NDC 44911-0147-01 - Lithium Carb

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
44911-0147
Requested NDC
44911-0147-01
Package NDCs from labels
44911-0147-1, 44911-0147-01
Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-02-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Lithium Carb - Energique, Inc. | Apotheca CompanyEnergique, Inc. | Apotheca Company2024-02-27HUMAN OTC DRUG LABEL

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 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

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

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 121 of 152 · 3,040 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Genuine First Aid Hand Sanitizer with Pump Ethyl AlcoholALCOHOLGFA Production (Xiamen) Co., Ltd.af84b665-260a-596f-e053-2995a90ac38c2024-10-15WarningsExact identifier
unii: 3K9958V90M
Genuine First Aid Hand Sanitizer Ethyl AlcoholALCOHOLGFA Production (Xiamen) Co., Ltd.af84bd67-4988-30e6-e053-2a95a90a8d932024-10-15WarningsExact identifier
unii: 3K9958V90M
HILL COUNTRY FARE HAND SANITIZER WITH ALOE FRAGRANCEALCOHOLH.E.Bc89b48e9-1746-874b-e053-2995a90ab0712024-10-15WarningsExact identifier
unii: 3K9958V90M
HEB Citrus Hand SanitizerALCOHOLH.E.B.c8ab20e5-6a20-5a6b-e053-2a95a90a247c2024-10-15WarningsExact identifier
unii: 3K9958V90M
EyS Eye WashWATEREyes-Plus LLC1443f6bf-3a77-4a19-8585-0ec58efe042f2024-10-15WarningsExact identifier
unii: 059QF0KO0R
Instant Hand Sanitizing WipeETHYL ALCOHOLMcKesson9f51a505-2d55-5c49-e053-2a95a90a24032024-10-14WarningsExact identifier
unii: 3K9958V90M
Eye WashWATER SOLUTIONKroger Company354402ad-581d-47e7-9fd3-933bef281ff42024-10-11WarningsExact identifier
unii: 059QF0KO0R
Insect Sting Relief PadBENZOCAINE, ALCOHOLHubei Changjian Medical Products Co., Ltd.6a269982-0e25-4c09-aef1-0b398bdc5ed42024-10-11WarningsExact identifier
unii: 3K9958V90M
Antiseptic Hand SanitizerALCOHOLHubei Changjian Medical Products Co., Ltd.b7f00c15-852f-45ce-9c60-70e0b80234f52024-10-11WarningsExact identifier
unii: 3K9958V90M
Eye WashWATERHubei Changjian Medical Products Co., Ltd.d57e1c5b-1edc-4a94-88bc-f9ecf347b7ea2024-10-11WarningsExact identifier
unii: 059QF0KO0R
AntisepticETHANOLMcKesson6637290d-6ae4-5a83-e053-2991aa0a81c62024-10-11WarningsExact identifier
unii: 3K9958V90M
Alcohol Disinfecting WipeALCOHOLMcKesson Medical-Surgical64a0063d-a5da-4a46-9dca-16e4dbdac85c2024-10-11WarningsExact identifier
unii: 3K9958V90M
MistALCOHOLDerma Glove2a0bcc4e-5114-4afc-91cb-cb4816a63db22024-10-09WarningsExact identifier
unii: 3K9958V90M
HandLOTIONDerma Gloveba9611a3-e2a4-4835-9ffe-aafe85a7cb9c2024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand ReliefLOTIONDerma Glove45d130c9-0835-45bb-b525-86a2119c87d12024-10-09WarningsExact identifier
unii: 3K9958V90M
MistALCOHOLDerma Gloveb5bfd7f0-0f96-459e-84d4-24b2081ae46f2024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand ReliefLOTIONDerma Glovee2f89d56-5624-4a94-8151-1edb508232ac2024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand RecoveryALCOHOLDerma Glove06f74478-57aa-4b8d-b888-55e1ee4fbd452024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand ReliefLOTIONDerma Gloved3926f48-3a42-42df-a850-47b3914ba3b62024-10-09WarningsExact identifier
unii: 3K9958V90M
MistALCOHOLDerma Glove7c21ee1c-ce2a-464b-8269-cdb3e59db0942024-10-09WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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