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 22:54:06

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 a 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.

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 description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1053429	water 99.1 % Ophthalmic Irrigation Solution	PSN	2
1053429	water 991 MG/ML Ophthalmic Irrigation Solution	SCD	2
1053429	water 99.05 % Ophthalmic Irrigation Solution	SY	2
1053429	water 99.1 % Ophthalmic Irrigation Solution	SY	2
1053429	water 99.1 ML per 100 ML Ophthalmic Irrigation Solution	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71271-100-03	2020-01-31	C162847	48780-1	9d75b9d1-1e48-f424-e053-dadaa90a57ce	Eyewash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71271-100-03	Eyewash	500 mL in 1 BOTTLE	LIQUID	500		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71271-100	EYEWASH (PURIFIED WATER) LIQUID [RELIANCE MEDICAL LTD]	2	Legacy NDC, 1 package rows	20180110_999cb2b0-89b0-4b24-805a-6cfc0f9ddda5.zip

Products#

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

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

Eyewash
PURIFIED WATER
WATER
SODIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71271-100	71271-100-03

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
Name	UNII	Kind
WATER	059QF0KO0R	ACTIB
SODIUM CHLORIDE	451W47IQ8X	IACT

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
1872b6d4-b171-4c2f-ad60-a1e7e21872d3			999cb2b0-89b0-4b24-805a-6cfc0f9ddda5	2018-01-09	Warnings	Exact identifier spl id: 1872b6d4-b171-4c2f-ad60-a1e7e21872d3 spl set id: 999cb2b0-89b0-4b24-805a-6cfc0f9ddda5

Reported adverse events (FAERS/openFDA)#

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