Buffered Eye-Lert

Dosage form: liquid
Ingredients: WATER 98mL in 100mL
Labeler: North Safety Products
NDC Code: 0498-0160

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Buffered Eye-Lert

Active ingredient

Purified water 98%

Purpose

Emergency eyewash and skin flush

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


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 
water liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-0160
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WATER (WATER) WATER98 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE 
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE 
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 
EDETATE DISODIUM 
BENZALKONIUM CHLORIDE 
Packaging
#Item CodePackage Description
1NDC:0498-0160-16473 mL in 1 BOTTLE, PLASTIC
2NDC:0498-0160-38946 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34906/06/2010
Labeler - North Safety Products (059980441)
Registrant - North Safety Products (059980441)
Establishment
NameAddressID/FEIOperations
North Safety Products 059980441manufacture

Revised: 07/2010
 
North Safety Products

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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