EYE CLEAN- eye wash liquid

Eye Clean by

Drug Labeling and Warnings

Eye Clean by is a Otc medication manufactured, distributed, or labeled by HART Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Purified Water 98.3%

PURPOSE

Purpose: Eyewash

INDICATIONS & USAGE

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

WARNINGS

Warnings: For external use only

DO NOT USE

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

When using this product:

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

STOP USE

Stop use and ask a doctor if you experience:

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

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 affeced eye as needed, controlling the rate of flow of solution by pressure on the bottle.

INACTIVE INGREDIENT

Inactive Ingredients: Boric Acid, Sodium Borate, Sodium Chloride

PRINCIPAL DISPLAY PANEL

EyeClean.jpg

INGREDIENTS AND APPEARANCE

EYE CLEAN 
eye wash liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50332-0201
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	98.3 mL  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: 50332-0201-3	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/1900
2	NDC: 50332-0201-1	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/1900
3	NDC: 50332-0201-4	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/1900
4	NDC: 50332-0201-6	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/1900
5	NDC: 50332-0201-8	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/1900

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	01/01/1900

Labeler - HART Health (069560969)

Registrant - Niagara Pharmaceuticals, Inc. (205477792)

Establishment
Name	Address	ID/FEI	Business Operations
Niagara Pharmaceuticals, Inc.		205477792	manufacture(50332-0201)