NEUTRAL-EYES- purified water 98.3% solution

Neutral-Eyes by

Drug Labeling and Warnings

Neutral-Eyes by is a Otc medication manufactured, distributed, or labeled by Western First Aid Safety. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Purified Water 98.3%

PURPOSE

Purpose

Eyewash

INDICATIONS & USAGE

Use For cleansing the eye to remove loose foreign
material

WARNINGS

Warnings

For external use only

Do not use■ if you experience any open wounds in or near the eyes
and get medical help right away
■ 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 experience
■ eye pain ■ changes in vision ■ continued redness
or irritation of the eye ■ condition worsens or persists

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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

INFORMATION FOR PATIENTS

Other information ■ for your protection, this
bottle has an imprinted white seal with black
printing”TAMPER EVIDENT SEAL” ■ do not use if
this seal is missing or broken ■ use before
expiration date marked on bottle ■ lot number is
printed on the bottle ■ store at 20º to 25º C [68º to
77º F]

INACTIVE INGREDIENT

Inactive ingredients boric acid, sodium borate,
sodium chloride

QUESTIONS

Questions? Call (800) 441-6774 8am to 5pm
PST Monday-Friday

Product Labeling

aramark

EYE WASH

Ophthalmic solution

INDUSTRIAL

NEUTRAL-EYES®

STERILE AND ISOTONIC FIRST AID TREATMENT

Mo. 708R23                       1 FL. OZ (30mL)

Made in Canada            Aramark Lenexa, KS 66219

1 FL OZ

4 FL OZ

8 FL OZ

16 FL OZ

32 FL OZ

res

INGREDIENTS AND APPEARANCE

NEUTRAL-EYES 
purified water 98.3% solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81238-6708
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	98.3 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81238-6708-1	30 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	02/15/2021
2	NDC: 81238-6708-3	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/15/2021
3	NDC: 81238-6708-4	118 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	02/15/2021
4	NDC: 81238-6708-6	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/15/2021
5	NDC: 81238-6708-8	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/15/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA	NDA022305	02/15/2021

Labeler - Western First Aid Safety (043861524)

Registrant - Western First Aid Safety (043861524)

Establishment
Name	Address	ID/FEI	Business Operations
Niagara Pharmaceuticals, inc.		205477792	manufacture(81238-6708) , label(81238-6708) , pack(81238-6708)