Active Ingredients
Lithium Bromatum 3xHPUS
The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.
Lithium Liquid
FDA Label NDC 60986-1019
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Marco Pharma International Llc. for the product Lithium (NDC 60986-1019). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, otc - keep out of reach of children, dosage, warnings, dosage & administration, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
For the temporary relief of symptoms due to depression, anxiety, and vertigo.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Dosage
Adults: Take 20 drops on the toungue or in water two to three times daily. Children receive 1/2 of the adult amount.
Warnings
If pregnant or breast-feeding, consult a health professional before use.
Dosage & Administration
(Read Suggested Use Section)
Inactive Ingredients
Ethyl alcohol (18% by vol.) and water.
Package Label.Principal Display Panel
Lithium.jpg
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