EyS Eye Wash description, usages, side effects, indications, overdosage, supplying and lots more!

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EyS Eye Wash

Eyes-Plus LLC

EyS Eye Wash


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredient

Purified water 98%

Purpose

Emergency eyewash and skin flush

Indications

For flushing the eyes to help relieve irritation, discomfort, burning, stinging, or itching by removing loose foreign material and air pollutants (smog or pollen).

Warnings

For external use only

  • To avoid contamination, do not touch tip of container to any surface
  • Do not reuse
  • Discard bottle after use

Do not use

  • If solution changes color or becomes cloudy
  • With contact lenses
  • If bottle is open or seal is broken

Stop use and consult a doctor if you experience

  • Eye pain
  • Changes in vision
  • Continued redness or irritation of the eye or if the condition worsens or persists

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.

Directions

  • To stream - twist off top and squeeze bottle. To pour - hold bottle securely, grip cap, and snap off.
  • Control rate of flow by pressure on the bottle.
  • Flush the affected eye(s) as needed.
  • Do not touch bottle tip to eye.
  • If necessary, continue flushing with emergency eyewash or shower.

Inactive Ingredients

benzalkonium chloride, edetate disodium dihydrate, sodium chloride, sodium phosphate dibasic heptahydrate, sodium phosphate monobasic monohydrate.

Questions or Comments?

Call Toll Free: (424) 263-5294

Store at 41-95°F (5-35°C)

PRINCIPAL DISPLAY PANEL - 480 ml Bottle Label

Tamper-evident cap: Do not use if twist-off top is broken or missing -Single use only

Eyes-PlusLLC

EyS

NDC 57349-913-16

Sterile Buffered Isotonic Solution

Eye Wash

Cleans, Refreshes & Soothes

Product Code: EyS-16
16 fl oz (480ml)

EyS Eye Wash

EyS Eye Wash

Water SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57349-913
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
water 0.98 mL

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
EDETATE DISODIUM
SODIUM CHLORIDE
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Sodium Phosphate, Monobasic, Monohydrate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57349-913-16 496 in 1 BOTTLE
2 NDC:57349-913-32 946 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-03-01


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Be sure to consult your doctor before taking any medication!
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