SODIUM CHLORIDE- sodium chloride solution/ drops
Walgreens

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Sodium Chloride 5%

Purpose

Hypertonicity Agent

Use

For temporary relief of corneal edema

Warnings

Do not use

this product except under the advice and supervision of a doctor
if imprinted seal on bottle is missing or broken
if solution changes color or becomes cloudy

When using this product

temporary burning and irritation upon being instilled into eye may occur
to avoid contamination, do not touch tip of container to any surface
replace cap after each use

Stop use and ask a doctor if

you experience eye pain
you experience changes in vision
redness or irritation of the eye continues
condition worsens or persists

Keep out of reach of children.

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

Directions

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

Other information

store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
keep tightly closed.

Inactive ingredients

Boric Acid, Hydrochloric Acid*, Hypromellose 2906, Methylparaben 0.23 mg (0.023%), Propylene Glycol, Propylparaben 0.1 mg (0.01%), Water for Injection, Sodium Borate, Sodium Hydroxide*. *May contain one or more of these ingredients to adjust pH (6.0 to 8.0).

Questions or Comments?

1-800-932-5676

Principal Display Panel Text for Container Label:

Well at

Walgreens NDC 0363-9040-00

STERILE

Sodium Chloride

Ophthalmic

Solution USP, 5%

Hypertonicity Eye Drops

0.5 FL OZ (15 mL)

Principal Display Panel Text for Container Label

Principal Display Panel Text for Carton Label:

Well at

Walgreens NDC 0363-9040-00

WALGREENS PHARMACIST RECOMMENDED≠

STERILE

Sodium Chloride

Ophthalmic

Solution USP, 5%

Hypertonicity Eye Drops

0.5 FL OZ (15 mL)

Compare to Muro 128®

active ingredient#

Principal Display Panel Text for Carton Label

SODIUM CHLORIDE
sodium chloride solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-9040
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Sodium Chloride (UNII: 451W47IQ8X) (Sodium Cation - UNII:LYR4M0NH37)	Sodium Chloride	50 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
Boric Acid (UNII: R57ZHV85D4)
Hypromelloses (UNII: 3NXW29V3WO)
Propylene Glycol (UNII: 6DC9Q167V3)
Sodium Borate (UNII: 91MBZ8H3QO)
Sodium Hydroxide (UNII: 55X04QC32I)
Hydrochloric Acid (UNII: QTT17582CB)
Water (UNII: 059QF0KO0R)
Methylparaben (UNII: A2I8C7HI9T)
Propylparaben (UNII: Z8IX2SC1OH)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0363-9040-00	1 in 1 CARTON	02/12/2013	12/31/2018
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part349	02/12/2013	12/31/2018

Labeler - Walgreens (008965063)

Revised: 10/2020

Document Id: 58e38d67-4661-4b3f-b103-70ec15f098cc

Set id: 69d1b3e9-60b9-4b0f-ac43-eb420395106f

Version: 5

Effective Time: 20201021

Walgreens