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
Manufacturer
Walgreen Company
Product type
HUMAN OTC DRUG
SPL set ID
d112a344-33cc-41d3-bae6-492631ebdba7
SPL ID
43f4dd02-20e9-ee0b-e063-6294a90ad917
Version
7
Effective date
2025-11-19
Source export date
2026-10-30
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 18:34:44
Harmonized routes table
Harmonized routes
OPHTHALMIC

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 For use in the eyes only Save box for complete information Do not use • except under the advice and supervision of a doctor. • if solution changes color or becomes cloudy. When using this product • keep tightly closed. • to avoid contamination, do not touch tip of container to any surface. • replace cap immediately after each use. • this product may cause temporary burning and irritation on being instilled into the eye. Stop use and ask a doctor if • you experience eye pain. • changes in your vision occur. • continued redness or irritation of the eye persists. • condition worsens or persists. Keep out of reach of children . If swallowed, 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.