Eye Wash

Manufacturer
NuCare Pharmaceuticals, Inc.
Effective date
2020-01-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:43:54

Label at a glance#

ProductEye Wash
Active ingredientWATER
Label structure12 sections

Storage and handling

Other information - store at 15° - 25°C (59° - 77°F) - keep tightly closed

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                        Purpose

Purified water (99.05%)............................Eyewash

OTC - PURPOSE SECTION

Uses

washes the eye to help relieve

- irritation

- stinging

- tching

by removing

- loose foreign material

- air pollutants (smog or pollen)

- chlorinated water

WARNINGS SECTION

Warnings

Do not use

if solution changes color or becomes cloudy

OTC - WHEN USING SECTION

When using this product

- remove contact lenses before using

- do not touch tip of container to any surface to avoid contamination

- replace cap after use

OTC - ASK DOCTOR SECTION

Stop use and ask doctor if

- you experience eye pain, changes in vision, continued redness or irritation of the eye

- condition worsens or persists

- you have open wounds in or near the eye

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 right away.

INDICATIONS & USAGE SECTION

Directions

- flush the affected eye(s) as needed

- control the rate of flow of solution by placing pressure on the bottle

OTC - WHEN USING SECTION

When using an eye cup

- rinse the cup with clean water immediately before each use

- avoid contamination of the rim and inside surfaces of the cup

- fill the cup half full and apply the cup to the affected eye(s), pressing tightly to prevent the escape of the liquid

- tilt the head backward. Open eyelids wide and rotate eyeball to ensure thorough bathing with the wash or lotion

- rinse the cup with clean water after each use

STORAGE AND HANDLING SECTION

Other information

- store at 15° - 25°C (59° - 77°F)

- keep tightly closed

INACTIVE INGREDIENT SECTION

Inactive ingredients

boric acid, edetate disodium, sodium borate, sodium chloride, sodium hydroxide and sorbic acid

DOSAGE & ADMINISTRATION SECTION

DISTRIBUTED BY

MAJOR PHARMACEUTICALS

31778 ENTERPRISE DRIVE

LIVONIA, MI 48150 USA

Made in Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pdppdp

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-974-04ML - Milliliter66267-97479680156-3229-41d2-b276-001b259fda0c12016-09-02
0904-6491-20ML - Milliliter0904-6491b5eceb32-19eb-4fba-8b01-afd2ccb3440312016-01-13

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66267-97466267-974-04
0904-6491

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
a22f6ee2-6a00-7f9d-e053-2a95a90a57e33b670818-602e-0fca-e054-00144ff88e882020-03-31WarningsExact identifier
spl set id: 3b670818-602e-0fca-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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