CVS Eyewash

Manufacturer: CVS | Tender Corporation
Effective date: 2020-11-24
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 23:00:59

Label at a glance#

ProductCVS Eyewash

Active ingredientWATER

Label structure9 sections

Dosage and administration

Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle.

Storage and handling

Store 36°F-104°F Use 59°F-86°F

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Purified Water USP 98.577% w/v

Purpose

OTC - PURPOSE SECTION

Eyewash

Use

INDICATIONS & USAGE SECTION

Use for flushing the eye to remove loose foreign material

Warnings

WARNINGS SECTION

To avoid contamination, do not touch tip of container to any surface.

Do not reuse.

Once opened, discard.

If you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists, consult a doctor.

Obtain immediate medical treatment for all open wounds in or near the eyes.

If solution changes color or becomes cloudy do not use nor, if twist-off Tamper Evident top is broken or missing.

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

Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Disodium EDTA

Polyhexanide

Sodium Chloride

Sodium Hydroxide

Sodium Phosphate, Dibasic

Sodium Phosphate, Monobasic

Storage and Handling

STORAGE AND HANDLING SECTION

Store 36°F-104°F

Use 59°F-86°F

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

boxvial

Products#

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

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

CVS Eyewash
Purified Water
A-Med brand First Aid Eye and Skin-Rinse
SODIUM CHLORIDE
SODIUM PHOSPHATE, DIBASIC DODECAHYDRATE
EDETATE DISODIUM
EDETIC ACID
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE
SODIUM HYDROXIDE
POLIHEXANIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69842-209	69842-209-10, 69842-209-12
59276-209	59276-209-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM CHLORIDE	451W47IQ8X	IACT
SODIUM PHOSPHATE, DIBASIC DODECAHYDRATE	E1W4N241FO	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE	5QWK665956	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
POLIHEXANIDE	322U039GMF	IACT
WATER	059QF0KO0R	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d26901a9-079a-9daa-e053-2995a90a70f4			5b1e83c8-e3b1-8793-e053-2991aa0ac79e	2021-12-05	Warnings	Exact identifier spl set id: 5b1e83c8-e3b1-8793-e053-2991aa0ac79e

Reported adverse events (FAERS/openFDA)#

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