EYE WASH- water solution

Eye Wash by

Drug Labeling and Warnings

Eye Wash by is a Otc medication manufactured, distributed, or labeled by GFA Production (Xiamen) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Purified Water 99.1%

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

Keep out of reach of children.

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

Stop use and ask a doctor if

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

Directions

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

Other information

not for use as contact lens solution

use before expiration date marked on the bottle

store at room temperature, 5° to 35°C (41° to 95°F)

Inactive ingredients

Benzalkonium chloride, sodium chloride

Package Labeling:

INGREDIENTS AND APPEARANCE

EYE WASH 
water solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50814-010
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	991 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50814-010-01	1 in 1 BOX	08/09/2016	12/31/2025
1		30 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/09/2016	12/31/2025

Labeler - GFA Production (Xiamen) Co., Ltd. (421256261)