Walgreens Lubricant Eye Solution

Manufacturer
WALGREEN CO
Effective date
2018-02-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:03:27

Label at a glance#

ProductWalgreens Lubricant Eye Solution
Active ingredientGLYCERIN, CARBOXYMETHYLCELLULOSE SODIUM
Label structure11 sections

Storage and handling

Other information use before expiration date marked on container store at 59-86°F (15-30°C) RETAIN THIS CARTON FOR FUTURE REFERENCE

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purpose

Carboxymethylcellulose sodium...............Eye Lubricant

Glycerin 0.9%...........................................Eye Lubricant

OTC - PURPOSE SECTION

Uses

  • For the temporary relief of burning and irritation due to dryness of the eye or exposure to wind or sun.
  • May be used as a protectant against further irritation

WARNINGS SECTION

Warnings

  • For external use only
  • To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
  • If solution changes color or becomes cloudy, do not use.

OTC - STOP USE SECTION

Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

INDICATIONS & USAGE SECTION

Directions

  • Instill 1 or 2 drops in the affected eye(s) as needed

STORAGE AND HANDLING SECTION

Other information

  • use before expiration date marked on container
  • store at 59-86°F (15-30°C)
  • RETAIN THIS CARTON FOR FUTURE REFERENCE

INACTIVE INGREDIENT SECTION

Inactive ingredients

benzalkonium chloride, boric acid, calcium chloride, magnesium chloride, potassium chloride, purified water, sodium borate, sodium citrate

DOSAGE & ADMINISTRATION SECTION

Distributed by:

Walgreens Co.

200 Wilmot Rd.

Deerfield, IL 60015

Made in South Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

986021986021

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

986022986022

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-60210363-6021-15, 0363-6021-30

Ingredients#

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

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

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
cddfaf3f-c497-7ac6-e053-2995a90ae47964a8aa75-b1dd-68cb-e053-2991aa0ae5c92021-10-08WarningsExact identifier
spl set id: 64a8aa75-b1dd-68cb-e053-2991aa0ae5c9

Reported adverse events (FAERS/openFDA)#

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