Sodium Chloride Hypertonicity

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 Hypertonicity
Generic name: SODIUM CHLORIDE
Manufacturer: CVS PHARMACY
Product type: HUMAN OTC DRUG
SPL set ID: d5cc6cd1-ddf8-4f5b-a021-204cdda0db94
SPL ID: 48727bb0-e2bc-1eab-e063-6394a90a1144
Version: 5
Effective date: 2026-01-15
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:49

Harmonized routes table
Harmonized routes
OPHTHALMIC

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		Sodium Chloride Hypertonicity	openfda.brand_name
generic name		SODIUM CHLORIDE	openfda.generic_name
manufacturer name		CVS PHARMACY	openfda.manufacturer_name
ndc	package	69842-285-35	openfda.package_ndc
ndc	product	69842-285	openfda.product_ndc
ndc11	package	69842028535	derived:openfda.package_ndc
rxcui		1298435	openfda.rxcui
spl id		48727bb0-e2bc-1eab-e063-6394a90a1144	id
spl set id		d5cc6cd1-ddf8-4f5b-a021-204cdda0db94	set_id
unii		451W47IQ8X	openfda.unii

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 external use only Do not use ▪ except under the advice and supervision of a doctor When using this product ▪ it may cause temporary burning and irritation ▪ replace cap after use ▪ to avoid contamination do not touch tip of container to any surface Stop use and ask a doctor if ▪ condition worsens or persists for more than 72 hours ▪ you experience eye pain, changes in vision, continued redness or irritation of the eye

Reported adverse events (FAERS/openFDA)#

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