BSS

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: BSS
Generic name: BALANCED SALT SOLUTION
Manufacturer: Alcon Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 4bd4d59c-eb3b-4a5e-9eb7-ae95b0a92bea
SPL ID: f56f90e2-cd68-445b-b8fb-74a53f0f2ca6
Version: 15
Effective date: 2024-01-25
Source export date: 2026-10-27
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/9122bd1bdced046e8f62ea012d80757473b7d83ea1faeea61faef490e06fd630/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:09:44

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	NDA	020742	derived:openfda.application_number
application number		NDA020742	openfda.application_number
brand name		BSS	openfda.brand_name
generic name		BALANCED SALT SOLUTION	openfda.generic_name
manufacturer name		Alcon Laboratories, Inc.	openfda.manufacturer_name
ndc	package	0065-0795-50	openfda.package_ndc
ndc	package	0065-0795-30	openfda.package_ndc
ndc	package	0065-0795-25	openfda.package_ndc
ndc	package	0065-0795-15	openfda.package_ndc
ndc	product	0065-0795	openfda.product_ndc
ndc11	package	00065079530	derived:openfda.package_ndc
ndc11	package	00065079515	derived:openfda.package_ndc
ndc11	package	00065079525	derived:openfda.package_ndc
ndc11	package	00065079550	derived:openfda.package_ndc
rxcui		806396	openfda.rxcui
rxcui		806392	openfda.rxcui
spl id		f56f90e2-cd68-445b-b8fb-74a53f0f2ca6	id
spl set id		4bd4d59c-eb3b-4a5e-9eb7-ae95b0a92bea	set_id
unii		02F3473H9O	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		1Q73Q2JULR	openfda.unii
unii		660YQ98I10	openfda.unii
unii		M4I0D6VV5M	openfda.unii
unii		4550K0SC9B	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 • NOT FOR INJECTION OR INTRAVENOUS INFUSION. • Do not use unless product is clear, seal is intact, and container is undamaged. • Do not use if product is discolored or contains a precipitate. • SINGLE patient use only. The contents of this bottle should not be used in more than one patient. • This solution contains no preservative, unused contents should be discarded.

Adverse reactions cross-check#

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

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTIONS Irrigation or any other trauma to the corneal endothelium may result in corneal swelling or bullous keratopathy. Post-operative inflammatory reactions as well as incidents of corneal edema and corneal decompensation have been reported.

Reported adverse events (FAERS/openFDA)#

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

BSS