MEDI-FIRST EYEWASH- water solution
Unifirst First Aid Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Purified water 98.3%

Purpose

Eyewash

Use

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

Warnings

For external use only

Do not use

if you experience any open wounds in or near the eyes and obtain immediate medical treatment
if solution changes color or becomes cloudy

When using this product

to avoid contamination, do not touch tip of container to any surface
do not reuse
once opened, discard

Stop use and ask a doctor if

You have any of the following

changes in vision
eye pain
condition worsens or persists
continued redness or irritation of the eye

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

pull cover off cap
avoid contamination of the rim and inside surface of the eyecup
place eyecup surface to the affected eye, pressing tightly to prevent the escape of the liquid and tilt the head backward to pour liquid out
open eyelids wide and rotate eyeball while controlling the rate of flow of solution by pressing the bottle to ensure thorough bathing with the wash

Other information

lot number is printed on the bottle
store at 20º to 25º C [68º to 77º F]
do not use if tamper evident ring is broken
use before expiration date marked on bottle

Inactive ingredients

boric acid, sodium borate, sodium chloride

Questions?

Call 800-634-7680

Medi-First Niagara Eyewash Label

Medi-First®

Purified Water, 98.3%

Ophthalmic Solution

Eyewash

NDC 47682-199-26

Single Use

Sterile Eyecup Attached

Manufactured for

Medique Products

17080 Alico Commerce Ct.

Fort Myers, FL 33967

Made in Canada

Reorder #21526

Sterile Solution

32 Fl Oz [946 mL]

3 47682 21526 2

MEDI-FIRST EYEWASH
water solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-199
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	0.929 g in 946 mL

Ingredient Name	Strength
Inactive Ingredients
BORIC ACID (UNII: R57ZHV85D4)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47682-199-11	473 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	05/01/2014	03/01/2018
2	NDC:47682-199-26	946 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	05/01/2014	10/01/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part349	05/01/2014	03/01/2018

Labeler - Unifirst First Aid Corporation (832947092)

Name	Address	ID/FEI	Business Operations
Establishment
Niagara Pharmaceuticals Inc.		205477792	manufacture(47682-199)

Revised: 5/2018

Document Id: 6b2669ca-5222-291b-e053-2991aa0a5d60

Set id: cf1786ae-2f92-4928-b399-aa83f659ff75

Version: 3

Effective Time: 20180501

Unifirst First Aid Corporation