FDA.reportPublic FDA data

NDC 70518-1481-01 - Lithium Carbonate

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
70518-1481
Requested NDC
70518-1481-01
Package NDCs from labels
70518-1481-0, 70518-1481-1, 70518-1481-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-07-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Lithium Carbonate - REMEDYREPACK INC.REMEDYREPACK INC.2026-07-06HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2021-02-19These highlights do not include all the information needed to use LITHIUM and LITHIUM CARBONATE safely and effectively. See full prescribing information for LITHIUM and LITHIUM CARBONATE. LITHIUM oral solution, for oral use LITHIUM CARBONATE tablets, for oral use LITHIUM CARBONATE capsules, for oral use Initial U.S. Approval: 1970
2021-02-19These highlights do not include all the information needed to use LITHIUM and LITHIUM CARBONATE safely and effectively. See full prescribing information for LITHIUM and LITHIUM CARBONATE. LITHIUM oral solution, for oral use LITHIUM CARBONATE tablets, for oral use LITHIUM CARBONATE capsules, for oral use Initial U.S. Approval: 1970
2021-01-29These highlights do not include all the information needed to use LITHIUM and LITHIUM CARBONATE safely and effectively. See full prescribing information for LITHIUM and LITHIUM CARBONATE. LITHIUM oral solution, for oral use LITHIUM CARBONATE tablets, for oral use LITHIUM CARBONATE capsules, for oral use Initial U.S. Approval: 1970
2021-01-29These highlights do not include all the information needed to use LITHIUM and LITHIUM CARBONATE safely and effectively. See full prescribing information for LITHIUM and LITHIUM CARBONATE. LITHIUM oral solution, for oral use LITHIUM CARBONATE tablets, for oral use LITHIUM CARBONATE capsules, for oral use Initial U.S. Approval: 1970

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-1481-0Lithium Carbonate30 in 1 BLISTER PACKTABLET309
70518-1481-1Lithium Carbonate30 in 1 BLISTER PACKTABLET309

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-1481LITHIUM CARBONATE TABLET [REMEDYREPACK INC.]7Current NDC, Legacy NDC, 2 package rows20250223_c84cce95-cfcb-4426-aac6-d2f48f946ada.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 5 of 15 · 285 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Kollourion Eyesalve EyewashPURIFIED WATER 98.3%Miracle Eye Pharmaceuticalsb56d2ab9-169b-b490-e053-2a95a90a80b32025-12-28WarningsExact identifier
unii: 059QF0KO0R
Lithium CarbonateLITHIUM CARBONATEGlenmark Pharmaceuticals Inc., USA63b3790f-a9b5-47f4-bae1-ddf8b43c13c12025-12-23Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
rxcui: 197893
rxcui: 197889
unii: 2BMD2GNA4V
Sterile WaterWATERProPharma Distribution386a0a2f-4ff7-f128-e063-6294a90a7d4d2025-12-18Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Firstep FirstflushEYEWASHEncon Safety Products, Inc.a44beb26-79ae-98bd-e053-2995a90a9b742025-12-09WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.beda35c3-9a8b-47ad-e053-2995a90a7b1b2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Easy Care First Aid EyewashWATERTender Corporationa070aac8-e6d2-ef10-e053-2a95a90aa5b12025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.e07a064b-f680-405c-bbcd-24fac430951e2025-11-24WarningsExact identifier
unii: 059QF0KO0R
ULINE EyewashEYEWASHNiagara Pharmaceuticals Inc.2d7f22d2-320b-6af1-e063-6294a90addc62025-11-24WarningsExact identifier
unii: 059QF0KO0R
Pur-WashEYEWASHNiagara Pharmaceuticals, Inc.0d43b1c1-2699-37f1-e054-00144ff88e882025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.777e1559-786f-8d54-e053-2991aa0aa98d2025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.7289103a-5cbf-42f4-8848-e827149a43ca2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERFresenius Kabi USA, LLCfd823bef-c14c-4708-a18a-8aaa8470412f2025-11-18Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
ALUMIZENGARLIC, AVENA SATIVA FLOWERING TOP, BERBERIS VULGARIS ROOT BARK, ARCTIUM LAPPA ROOT, PHYTOLACCA AMERICANA ROOT, SOLIDAGO VIRGAUREA FLOWERING TOP, ALUMINUM OXIDE, SILVER NITRATE, BARIUM CARBONATE, BERYLLIUM, CADMIUM, COPPER, HYDROFLUORIC ACID, INDIUM, IODINE, LITHIUM CARBONATE, MERCURIUS SOLUBILIS, NICKEL CARBONATE HYDROXIDE TETRAHYDRATE, NITROUS OXIDE, LEAD, SELENIUM, STRONTIUM CARBONATE, TITANIUM, ARSENIC TRIOXIDE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED.Natural Creations, Inc.4760ab09-1141-4944-b840-804ae6d86d2d2025-11-13WarningsExact identifier
unii: 2BMD2GNA4V
Lithium CarbonateLITHIUM CARBONATEAmerican Health Packagingd276da3c-9952-4674-a54d-b1258df71b8a2025-11-13Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 2BMD2GNA4V
Lithium CarbonateLITHIUM CARBONATEAmerican Health Packaging5ce5ebd2-f1b5-4c04-a7de-56a1b7eb81972025-11-13Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 2BMD2GNA4V
Natural Relief Arthritis TherapyAPIS MELLIFERA, SALICYLIC ACID, RUTA GRAVEOLENS, TOXICODENDRON PUBESCEN, LITHIUM CARBONATE, BRYONIA ALBA, CALCIUM FLUORIDETRP Company436f7af7-859e-f7af-e063-6294a90af5082025-11-12WarningsExact identifier
unii: 2BMD2GNA4V
Eyesaline Eyewash ConcentratePURIFIED WATERHoneywell Safety Products USA, Inc.3765c251-eb14-d60f-e063-6294a90a6a4d2025-11-12WarningsExact identifier
unii: 059QF0KO0R
Eyesaline Emergency EyewashPURIFIED WATERHoneywell Safety Products USA, Inc.37f244fd-c02f-e66a-e063-6394a90aed812025-11-12WarningsExact identifier
unii: 059QF0KO0R
STERILE WATERWATERHenry Schein, Inc.f4087143-9868-4308-b96c-43657ee8ec282025-11-07Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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