Active Ingredient (In Each Tablet)
SODIUM CHLORIDE, USP 1 GRAM
The following Structured Product Label (SPL) was submitted to the FDA by Gendose Pharmaceuticals, Llc for the product Sodium Chloride (NDC 77333-835). 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 ingredient (in each tablet), purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
SODIUM CHLORIDE, USP 1 GRAM
ELECTROLYTE REPLENISHER
NONE
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