Eyewash

Manufacturer
Reliance Medical Ltd
Effective date
2018-01-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:54:03

Label at a glance#

ProductEyewash
Active ingredientWATER
Label structure11 sections

Indications and uses

For cleansing the eye to remove loose foreign material.

Dosage and administration

• smoothly twist the lid in either direction to break the seal and remove the lid. • position the bottle above the eye and gently squeeze. • flush the affected eye as needed controlling the rate of flow of solution by pressure on the bottle. • cleanse the eye(s) with as much solution as required.

Storage and handling

• store between 5°C and 35°C (41° to 95° F). • use before expiry date. • do not use if seal is broken prior to use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Purified Water 99.1 %

Purpose

OTC - PURPOSE SECTION

Eyewash

Uses

INDICATIONS & USAGE SECTION

For cleansing the eye to remove loose foreign material.

Warnings

WARNINGS SECTION

For external use only.

Do not use

• if solution changes colour or becomes cloudy

• for injection

• as a contact lens solution.

When using the product

• do not re-use, once opened, discard.

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

Stop use and consult a doctor if

• you experience eye pain.

• changes in vision.

• continued redness or irritation of the eye.

• the condition worsens or persists.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

• If swallowed, get medical help or contact Poison Control Centre right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• smoothly twist the lid in either direction to break the seal and remove the lid. • position the bottle above the eye and gently squeeze.
• flush the affected eye as needed controlling the rate of flow of solution by pressure on the bottle. • cleanse the eye(s) with as much solution as required.

Other information

STORAGE AND HANDLING SECTION

• store between 5°C and 35°C (41° to 95° F).

• use before expiry date.

• do not use if seal is broken prior to use.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Sodium chloride.

Questions?

OTC - QUESTIONS SECTION

Call 1-844-405-7233. Monday - Friday, 9am - 5pm. You may also report serious side effects to this number.

SPL UNCLASSIFIED SECTION

MANUFACTURED FOR:

Reliance Medical LTD, Radnor Park Trading

Estate, Congleton, Cheshire, England, CW12 4XP, UK.

IMPORTED AND DISTRIBUTED BY:

Innovative Safety Supply USA Inc. 5150 West 76th St. Indianapolis,

IN, 46268 USA.

MADE IN CHINA

Compliance:

ANSI/ISEA Z358.1-2014

(As Personal Eye Wash Only)

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1053429water 99.1 % Ophthalmic Irrigation SolutionPSN2
1053429water 991 MG/ML Ophthalmic Irrigation SolutionSCD2
1053429water 99.05 % Ophthalmic Irrigation SolutionSY2
1053429water 99.1 % Ophthalmic Irrigation SolutionSY2
1053429water 99.1 ML per 100 ML Ophthalmic Irrigation SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71271-100-012020-01-31C16284748780-19d75b9d1-1e24-f424-e053-dadaa90a57ceEyewash
71271-100-022020-01-31C16284748780-19d75b9d1-1e24-f424-e053-dadaa90a57ceEyewash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71271-100-01Eyewash25 in 1 CARTONLIQUID252
71271-100-01Eyewash20 mL in 1 BOTTLELIQUID202
71271-100-02Eyewash250 mL in 1 BOTTLELIQUID2502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71271-100EYEWASH (PURIFIED WATER) LIQUID [RELIANCE MEDICAL LTD]2Legacy NDC, 3 package rows20180110_41dee46f-008d-43b3-b1a6-f161e2d2a2cd.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71271-10071271-100-01, 71271-100-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RACTIB
SODIUM CHLORIDE451W47IQ8XIACT

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
03e127f6-575c-4b15-a59b-2ac1eaecbf9f41dee46f-008d-43b3-b1a6-f161e2d2a2cd2018-01-09WarningsExact identifier
spl id: 03e127f6-575c-4b15-a59b-2ac1eaecbf9f
spl set id: 41dee46f-008d-43b3-b1a6-f161e2d2a2cd

Reported adverse events (FAERS/openFDA)#

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