Walgreens Lubricating Eye Drops 0.5 oz (NBE Thera Tears) 878000 (2018)

Manufacturer
Walgreen Company
Effective date
2018-03-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:55:11

Label at a glance#

ProductWalgreens Lubricant Eye
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure11 sections

Storage and handling

Other information Store at room temperature.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purpose

Sodium carboxymethycellulose 0.25%..................................Lubricant

OTC - PURPOSE SECTION

Uses

  • As a lubricant to relieve dryness of the eye
  • As a protectant against further irritation of the eye
  • For temporary relief of burning, irritation, and discomfort including exposure to wind or sun

WARNINGS SECTION

Warnings

For external use only

  • To avoid contamination do not touch tip of opened container to any surface. Replace cap after using.

OTC - DO NOT USE SECTION

Do not use

  • if solution changes color or becomes cloudy.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • you experience eye pain, changes in vision, continued redness or irritation
  • condition worsens or persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

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

INDICATIONS & USAGE SECTION

Directions

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

STORAGE AND HANDLING SECTION

Other information

  • Store at room temperature.

INACTIVE INGREDIENT SECTION

Inactive ingredients

benzalkonium chloride, boric acid, calcium chloride, magnesium chloride, potassium chloride, sodium bicarbonate, sodium borate, sodium chloride, sodium dihydrogen phosphate monohydrate, water

DOSAGE & ADMINISTRATION SECTION

Distributed by:

Walgreen Co.

200 Wilmont Rd.

Deerfield, IL 60015

Made in South Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

placeholderplaceholder

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-00840363-0084-15

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
d105df6e-49b8-ead7-e053-2a95a90a3b6167dfba36-b8ea-7d93-e053-2a91aa0a429f2021-11-17WarningsExact identifier
spl set id: 67dfba36-b8ea-7d93-e053-2a91aa0a429f

Reported adverse events (FAERS/openFDA)#

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