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Medi-First

Unifirst First Aid Corporation


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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

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

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 the rim and inside surface of the eyecup
  • place eyecup surface to the affected eye, pressing tightly to prevent the escape of the liquid and tilt the head backward to pour liquid out
  • open eyelids wide and rotate eyeball while controlling the rate of flow of solution by pressing the bottle to ensure thorough bathing with the wash

Other information

  • lot number is printed on the bottle
  • store at 20º to 25º C [68º to 77º 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 800-634-7680

Medi-First Niagara Eyewash Label

Medi-First®

Purified Water, 98.3%

Ophthalmic Solution

Eyewash

NDC 47682-199-26

Single Use

Sterile Eyecup Attached

Manufactured for

Medique Products

17080 Alico Commerce Ct.

Fort Myers, FL 33967

Made in Canada

Reorder #21526

Sterile Solution

32 Fl Oz [946 mL]

3 47682 21526 2

Medi-First

Water SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:47682-199
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
water 0.929 g

Inactive Ingredients

Ingredient Name Strength
BORIC ACID
SODIUM BORATE
SODIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:47682-199-11 473 in 1 BOTTLE, UNIT-DOSE
2 NDC:47682-199-26 946 in 1 BOTTLE, UNIT-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2014-05-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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