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 114 of 153 · 3,045 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Absolutely Natural Rosemary and Mint Hand SanitizerETHYL ALCOHOLAbsolutely Natural, Inc.a7be8b58-8f3e-46ed-ae4d-45f093c98dc32024-12-11WarningsExact identifier
unii: 3K9958V90M
ZOEY naturals English Garden HAND SANITIZERETHYL ALCOHOLAbsolutely Natural0c7d0d85-b919-4f47-9888-1ccc91054edf2024-12-11WarningsExact identifier
unii: 3K9958V90M
Zoey Naturals Lemon Squeeze Hand SanitizerETHYL ALCOHOLAbsolutely Natural, Inc.c119069c-092e-49ca-8f89-11fb75c768402024-12-11WarningsExact identifier
unii: 3K9958V90M
MELLOW HAND SANITIZER ALOEETHYL ALCOHOLL.e.d. Cosmetics, Inc.4377ba5e-21f6-407e-9b8c-25e3c6321a5b2024-12-10WarningsExact identifier
unii: 3K9958V90M
Fendall Pure FlowPURIFIED WATERHoneywell Safety Products USA, Inc.afda6fc3-7615-b0be-e053-2995a90a62082024-12-10WarningsExact identifier
unii: 059QF0KO0R
CVS Hand SanitizerALCOHOLCVSb5faeb31-67c7-2000-e053-2995a90a14092024-12-10WarningsExact identifier
unii: 3K9958V90M
QUALITY CHOICE INSTANT HAND SANITIZERETHYL ALCOHOLL.e.d. Cosmetics, Inc.4065c34c-d1ca-49bd-9fba-dfa21011592f2024-12-10WarningsExact identifier
unii: 3K9958V90M
QUALITY CHOICE INSTANT HAND SANITIZERETHYL ALCOHOLL.e.d. Cosmetics, Inc.ec37da5a-8ef7-474b-a5ec-b5edcee03f9d2024-12-10WarningsExact identifier
unii: 3K9958V90M
CSI E3 Hand SanitizerALCOHOLCentral Solutions Incaa07bb62-ef07-99e4-e053-2995a90ae4a82024-12-09WarningsExact identifier
unii: 3K9958V90M
DermaCen Instant Hand SanitizerALCOHOLCentral Solutions Inc36783d30-a222-40fe-a5ea-61a2842a34c92024-12-09WarningsExact identifier
unii: 3K9958V90M
DermaCen Instant Hand Sanitizer with AloeALCOHOLCentral Solutions Incdc6191ae-841f-48b6-b454-72d8d43fdcce2024-12-09WarningsExact identifier
unii: 3K9958V90M
DERMACEN FOAMING INSTANT HAND SANITIZER WITH ALOEALCOHOLCentral Solutions Incd56b9930-b8b0-ad72-e053-2a95a90af5902024-12-09WarningsExact identifier
unii: 3K9958V90M
Guard 2U Hand SanitizerGUARD 2U HAND SANITIZERAmerican Industries, Inc.f41cf3f4-6c6e-7354-e053-2a95a90affcc2024-12-08WarningsExact identifier
unii: 3K9958V90M
San-A-GelSAN-A-GELMisco Industrial, LLCdeac5e37-e1a0-5b4b-e053-2a95a90a9d5b2024-12-08WarningsExact identifier
unii: 3K9958V90M
ApplauseINSTANT HAND SANITIZERQuestSpecialty Corporation774657f1-5c39-2fed-e053-2991aa0a90642024-12-08WarningsExact identifier
unii: 3K9958V90M
Hand SanitizerHAND SANITIZERFehr Bros. Industries Inceac3f46a-1b61-c4b2-e053-2995a90ae7022024-12-08WarningsExact identifier
unii: 3K9958V90M
SaniTex 60SANITEX 60Solutex, Inc.d57827ec-f724-5081-e053-2a95a90adaaf2024-12-08WarningsExact identifier
unii: 3K9958V90M
Han-SanHAN-SANPro-Line Industrial Productsbd4a5c7e-af8b-d08d-e053-2995a90ac7722024-12-08WarningsExact identifier
unii: 3K9958V90M
Gel Antiseptic HandwashGEL ANTISEPTIC HANDWASHShop Bee's Wax LLCbdac168b-5d58-69ba-e053-2995a90aa5a42024-12-08WarningsExact identifier
unii: 3K9958V90M
InstantINSTANTDetco Industriesbd9a0b41-4861-adfc-e053-2a95a90ae7a02024-12-08WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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