Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent

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: Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent
Generic name: SODIUM CHLORIDE
Manufacturer: Altaire Pharmaceuticals Inc.
Product type: HUMAN OTC DRUG
SPL set ID: e13fd053-9420-490c-a43e-e14b0930cb4e
SPL ID: fc39d7b1-cea0-4702-89bd-bf63adbeb675
Version: 1
Effective date: 2026-03-18
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 05:26:04

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		Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent	openfda.brand_name
generic name		SODIUM CHLORIDE	openfda.generic_name
manufacturer name		Altaire Pharmaceuticals Inc.	openfda.manufacturer_name
ndc	package	59390-184-50	openfda.package_ndc
ndc	product	59390-184	openfda.product_ndc
ndc11	package	59390018450	derived:openfda.package_ndc
rxcui		1298435	openfda.rxcui
spl id		fc39d7b1-cea0-4702-89bd-bf63adbeb675	id
spl set id		e13fd053-9420-490c-a43e-e14b0930cb4e	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 use in the eye s only. • Retain carton for full product drug facts. Do not use this product except under the advice and supervision of a doctor. When using this product • avoid contamination, do not touch tip of container to any surface. • replace cap 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 vision, continued redness or irritation of the eye. • the condition worsens or persists for more than 72 hours. KEEP THIS AND ALL DRUGS OUT OF THE 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.