Buffered Eye-Lert description, usages, side effects, indications, overdosage, supplying and lots more!

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Buffered Eye-Lert

North Safety Products
North Safety Products

Buffered Eye-Lert


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Purified water 98%

Purpose

Emergency eyewash and skin flush

Buffered Eye-Lert Uses

for flushing the eye and skin to reduce chances of severe injury caused by acid, alkali or particulate contamination.

Warnings

For external use only

Do not use

  • for injection
  • in intraocular surgery
  • internally
  • if solution changes color or becomes cloudy

When using this product

  • 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

Ask doctor if you have

  • eye pain
  • changes in vision
  • redness or irritation of the eye after use
  • an injury caused by an alkai
  • condition worsens or persists

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

Directions

  • do not dilute solution or reuse bottle
  • hold container a few inches above the eye or skin
  • control flow of solution by pressure on bottle
  • flush affected area as needed a minimum of 20 minutes


Buffered Eye-Lert Other information

  • tamper evident: do not use if twist off top is broken or missing
  • not for use as a contact lens solution
  • twist cap to open
  • use before expiration date marked on bottle
  • store at room temperature, 15o to 30oC  (59o to 86o)

Inactive ingredients

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

Questions

Questions or comments?   Call toll free number 1-800-130-4110

Principal Display Panel

Buffered Eye-Lert

Buffered Eye-Lert

Water LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0498-0160
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
water 98 mL

Inactive Ingredients

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0498-0160-16 473 in 1 BOTTLE, PLASTIC
2 NDC:0498-0160-38 946 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2010-06-06


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