Altachlore 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
Altachlore Sodium Chloride Hypertonicity
Generic name
SODIUM CHLORIDE
Manufacturer
Altaire Pharmaceuticals Inc.
Product type
HUMAN OTC DRUG
SPL set ID
dc0d94d8-4475-4956-8ded-bdb9496074e4
SPL ID
0c0e9c0d-61f5-e63b-e063-6294a90ac0d9
Version
4
Effective date
2023-12-09
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:35:23
Harmonized routes table
Harmonized routes
OPHTHALMIC

Warnings cross-check#

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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.