EYEWASH- purified water liquid

Eyewash by

Drug Labeling and Warnings

Eyewash by is a Otc medication manufactured, distributed, or labeled by Reliance Medical Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Purified Water 99.1 %

Purpose

Eyewash

Uses

For cleansing the eye to remove loose foreign material.

Warnings

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.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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

Directions

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

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

Sodium chloride.

Questions?

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

INGREDIENTS AND APPEARANCE

EYEWASH 
purified water liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71271-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	0.991 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71271-100-01	25 in 1 CARTON	07/03/2017
1		20 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 71271-100-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/03/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	07/03/2017

Labeler - Reliance Medical Ltd (349044854)