Eye Wash

Manufacturer: GFA Production (Xiamen) Co., Ltd.
Effective date: 2024-10-09
Label type: HUMAN OTC DRUG LABEL
Version: 12
Source: legacy-cache
Hydrated at: 2026-08-01 20:53:09

Label at a glance#

ProductEye Wash

Active ingredientWATER

Label structure7 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Purified Water 99.1%

Purpose

OTC - PURPOSE SECTION

Eyewash

Use

INDICATIONS & USAGE SECTION

For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

if solution changes color or becomes cloudy

When using this product

OTC - WHEN USING SECTION

• to avoid contamination, do not touch tip of container to any surface • do not reuse • once opened, discard • obtain immediate medical treatment for all open wounds in or near the eyes

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.

Stop use and ask a doctor if

OTC - STOP USE SECTION

• you experience: • eye pain • changes in vision • continued redness • irritation of the eye • condition worsens or persists

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

SPL UNCLASSIFIED SECTION

• not for use as contact lens solution

• use before expiration date marked on the bottle

• store at room temperature, 5° to 35°C (41° to 95°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Benzalkonium chloride, sodium chloride

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Eye wash

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50814-010	EYE WASH (WATER) SOLUTION [GFA PRODUCTION (XIAMEN) CO., LTD.]	12	Unmatched	20241010_51464ae1-e1ba-44ff-adad-7dde9bc2c364.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Eye Wash
WATER
BENZALKONIUM CHLORIDE
SODIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50814-010	50814-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	IACT
SODIUM CHLORIDE	451W47IQ8X	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
24075ae8-7010-07f9-e063-6294a90a61e0			51464ae1-e1ba-44ff-adad-7dde9bc2c364	2024-10-09	Warnings	Exact identifier spl id: 24075ae8-7010-07f9-e063-6294a90a61e0 spl set id: 51464ae1-e1ba-44ff-adad-7dde9bc2c364

Reported adverse events (FAERS/openFDA)#

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