Home DailyMed f4a1d451-33ad-4df3-ae68-58cfbfccfa89 Lithium Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Marco Pharma International LLC. | Nestmann Pharma GmbH
Effective date 2026-01-12
Label type HUMAN OTC DRUG LABEL
Version 6
Source full-release
Hydrated at 2026-06-01 02:36:47 Label at a glance# Product Lithium
Active ingredient LITHIUM BROMIDE
Label structure 2 sections
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60986-1019-3 Lithium 50 mL in 1 BOTTLE, GLASS LIQUID 50 6 60986-1019-4 Lithium 100 mL in 1 BOTTLE, GLASS LIQUID 100 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII SPL version Uploaded LITHIUM BROMIDE ACTIVE INGREDIENT 864G646I84 1 LITHIUM BROMIDE ACTIVE MOIETY 864G646I84 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M 1 WATER INACTIVE INGREDIENT 059QF0KO0R 1
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 6 matching rows.
Lithium Lithium Bromatum WATER ALCOHOL LITHIUM BROMIDE LITHIUM CATION Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 3 matching rows.
Inactive ingredient matches# Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
Inactive ingredient links page 1 of 1 · 3 matching rows.
DailyMed ingredient, IID ingredient, UNII table DailyMed ingredient IID ingredient UNII Dosage form / route Potency Maximum daily exposure Match ALCOHOL ALCOHOL 3K9958V90M LIQUID / ORAL 3563 mg Exact identifier — unii+route+dosage form 3 equally ranked IID candidates ALCOHOL ALCOHOL 3K9958V90M LIQUID / ORAL 3563 mg Exact identifier — unii+route+dosage form 3 equally ranked IID candidates ALCOHOL ALCOHOL 3K9958V90M LIQUID / ORAL 3563 mg Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
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.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
