DYNAMIC EYEWASH WITH EYECUP- water solution

Dynamic Eyewash with Eyecup by

Drug Labeling and Warnings

Dynamic Eyewash with Eyecup by is a Otc medication manufactured, distributed, or labeled by Dynamic Safety International, Niagara Pharmaceuticals Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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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

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

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 rim and inside surfaces of the eyecup

place eyecup surface to the affected eye, pressing tightly to prevent the escape of the liquid and tilt the head backward

open eyelids wide and rotate eyeball while controlling the rate of flow of solution by pressure on the bottle to ensure thorough bathing with the wash

Other information

• lot number is printed on the bottle
• store at 20° to 25° C [68° to 77° 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 1-877-446-3278 9 a.m. to 5 p.m. EST Mon-Fri

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Manufactured by:
Niagara Pharmaceuticals Inc.
60 Innovation Dr.
Flamborough ON L9H 7P3

PRINCIPAL DISPLAY PANEL - DRUG FACTS

INGREDIENTS AND APPEARANCE

DYNAMIC EYEWASH WITH EYECUP 
water solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72745-101
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	929 g  in 946 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72745-101-32	946 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	12/17/2018
2	NDC: 72745-101-16	473 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	12/17/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA	NDA022305	12/17/2018

Labeler - Dynamic Safety International (244256769)

Registrant - Niagara Pharmaceuticals Inc. (205477792)

Establishment
Name	Address	ID/FEI	Business Operations
Niagara Pharmaceuticals Inc.		205477792	manufacture(72745-101)