FDA.reportPublic FDA data

moisture eyes lubricant eye drops

Manufacturer
Costco Wholesale Company | Bausch & Lomb Incorporated
Effective date
2024-09-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:54:29

Label at a glance#

Productmoisture eyes lubricant eye drops
Active ingredientPOVIDONE, UNSPECIFIED
Label structure10 sections

Indications and uses

■ relieves dryness of the eye ■ prevents further irritation

Dosage and administration

■ Instill 1 or 2 drop(s) in the affected eye(s) as needed or as directed by your doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Povidone (2.0%)

Purpose

OTC - PURPOSE SECTION

Lubricant

Uses

INDICATIONS & USAGE SECTION

■ relieves dryness of the eye
■ prevents further irritation

Warnings

WARNINGS SECTION

For external use only.

Do not use

WARNINGS SECTION

■ if solution changes color or becomes cloudy

When using this product

WARNINGS SECTION

■ do not touch tip of container to any surface to avoid contamination
■ remove contact lenses before using
■ replace cap after using

Stop use and ask a doctor if you experience

WARNINGS SECTION

■ eye pain
■ change in vision
■ continued redness or irritation of the eye
■ or if condition worsens or lasts more than 72 hours

If pregnant or breastfeeding, ask a health professional before use.

WARNINGS SECTION

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 drop(s) in the affected eye(s) as needed or as directed by your doctor

Other information

OTHER SAFETY INFORMATION

■ Storage: 15°-25°C (59°-77°F)

■ Use before expiration date marked on the carton or bottle

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzalkonium chloride (0.005%), boric acid, edetate disodium dihydrate, purified water, sodium borate, sodium chloride, tyloxapol. Hydrochloric acid and/or sodium hydroxide may be used to adjust pH.

Questions?

OTC - QUESTIONS SECTION

[phone icon] Call:1-800-774-2678

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KIRKLAND
Signature

moisture
eyes
LUBRICANT EYE DROPS

LONG LASTING
■ Dry Eye Therapy
■ Comforts
■ Moisturizes

Sterile          0.5 FL OZ EA (15 mL EA) 5 BOTTLES

carton.jpg
carton.jpg

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
63981-00263981-002-05

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
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
BORIC ACIDR57ZHV85D4IACT
EDETATE DISODIUM7FLD91C86KIACT
WATER059QF0KO0RIACT
SODIUM BORATE91MBZ8H3QOIACT
SODIUM CHLORIDE451W47IQ8XIACT
TYLOXAPOLY27PUL9H56IACT
HYDROCHLORIC ACIDQTT17582CBIACT
SODIUM HYDROXIDE55X04QC32IIACT
POVIDONE, UNSPECIFIEDFZ989GH94EACTIB

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
2c6208d6-c9f7-a6f8-e063-6394a90a4815d2d6d830-bc0e-4838-bde9-90250f27e6512025-01-23WarningsExact identifier
spl set id: d2d6d830-bc0e-4838-bde9-90250f27e651

Reported adverse events (FAERS/openFDA)#

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