Sodium Chloride

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Sodium Chloride
Generic name
SODIUM CHLORIDE TABLETS
Manufacturer
Kesin Pharma Corporation
Product type
HUMAN OTC DRUG
SPL set ID
2f107592-10c5-ef3b-e063-6394a90a7c0a
SPL ID
43cf75a9-e660-c580-e063-6394a90a0b87
Version
2
Effective date
2025-11-17
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:25:33
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Warnings Do not use Do not use without consulting a physician Ask a physician before use Ask a physician before use if you have a sodium restricted diet due to multiple organ diseases Stop use and ask a physician Stop use and ask a physician if symptoms of heat cramps continue for more than 24 hours If pregnant or breast-feeding If pregnant or breast-feeding, ask a health professional before use Keep out of reach of children. Keep out of reach of children. Overdose In case of overdose, get medical help or contact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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