FDA.reportPublic FDA data

Walgreens Sodium Chloride Ophthalmic Solution

Manufacturer
Walgreen Company
Effective date
2025-11-19
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:27:25

Label at a glance#

ProductSodium Chloride
Active ingredientSODIUM CHLORIDE
Label structure10 sections

Dosage and administration

• instill 1 or 2 drops in the affected eye(s) every 3 to 4 hours, or as directed by a doctor.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Walgreen’s Sodium Chloride Ophthalmic

 Solution, 5% Hypertonicity Eye Drops 15mL  

NDC 0363-0193-13

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride 5%

Purpose

OTC - PURPOSE SECTION

Hypertonicity Agent

Use

INDICATIONS & USAGE SECTION

• For the temporary relief of corneal edema.

Warnings

WARNINGS SECTION

For use in the eyes only

Save box for complete information

Do not use 

OTC - DO NOT USE SECTION

• except under the advice and supervision of a doctor.

• if solution changes color or becomes cloudy.

When using this product

OTC - WHEN USING SECTION

• 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  

OTC - STOP USE SECTION

• 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• instill 1 or 2 drops in the affected eye(s) every 3 to 4 hours, or as directed by a doctor.

Other information

OTHER SAFETY INFORMATION

• replace cap after using and keep tightly closed.

• store at 15° to 30°C (59° to 86°F).

• remove contact lenses before using.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Boric Acid, Hypromellose, Methylparaben, Propylene Glycol, Propylparaben, Sodium Borate, and Water for injection. Sodium Hydroxide and/or Hydrochloric Acid may be added to adjust pH.

Questions?

OTC - QUESTIONS SECTION

• 1-800-925-4733  • 9am – 5pm EST Monday - Friday

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens

NDC 0363-0193-13

Sodium Chloride

Ophthalmic

Solution, 5%

Hypertonicity

Eye Drops

0.5 FL OZ (15 mL)

CartonCarton

CartonCarton

LabelLabel

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
730780sodium chloride 5 % Ophthalmic SolutionPSN7
730780sodium chloride 0.854 MEQ/ML Ophthalmic SolutionSCD7
730780NaCl 0.854 MEQ/ML Ophthalmic SolutionSY7
730780NaCl 5 % Ophthalmic SolutionSY7

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
SODIUM CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130311917214177GTIN-13: 0311917214177
EAN-13: 0311917214177
GTIN-12: 311917214177
UPC-A: 311917214177
GTIN storage (14 digits): 00311917214177		Hypertonicity Eye Drops Carton.jpg, WAG_EE_662718_HypertonicityEyeDrops_BOX_TRPr3_F-OL.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
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fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
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6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-0193-132025-12-20C16284748780-11e7a6dab-19f1-a2ce-e063-dadaa90aadf7Walgreens Sodium Chloride Ophthalmic Solution
0363-0193-132024-07-30C16284748780-11e7a6dab-19f1-a2ce-e063-dadaa90aadf7Walgreens Sodium Chloride Ophthalmic Solution

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0193-13Sodium Chloride15 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS157
0363-0193-13Sodium Chloride1 in 1 BOXSOLUTION/ DROPS17

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-0193-13ML - Milliliter0363-01934efcbdfb-3131-47f0-9c61-e285f41878bb12022-06-06

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-01930363-0193-13

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BORIC ACIDR57ZHV85D4IACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
METHYLPARABENA2I8C7HI9TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PROPYLPARABENZ8IX2SC1OHIACT
SODIUM BORATE91MBZ8H3QOIACT
WATER059QF0KO0RIACT
SODIUM HYDROXIDE55X04QC32IIACT
HYDROCHLORIC ACIDQTT17582CBIACT
SODIUM CHLORIDE451W47IQ8XACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sodium ChlorideSODIUM CHLORIDEWalgreen Companyd112a344-33cc-41d3-bae6-492631ebdba72025-11-19WarningsExact identifier
ndc (package): 0363-0193-13
ndc (product): 0363-0193
ndc11 (package): 00363019313
spl id: 43f4dd02-20e9-ee0b-e063-6294a90ad917
spl set id: d112a344-33cc-41d3-bae6-492631ebdba7

Reported adverse events (FAERS/openFDA)#

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