EYESALINE CONCENTRATE- water liquid 
Sperian Eye & Face Protection Inc.

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.

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Sperian Eyesaline Concentrate

Active Ingredient

Purified water 93%

Purpose

Eyewash

Uses

Warnings

For external use only- Obtain immidiate medical treatment for all open wounds in or near the eyes. To avoid contamination, do not touch tip of container to any surface. Replace cap after use.

Do not use

  • in concentrated form
  • while wearing contact lenses
  • if solution changes color or becomes cloudy
  • for injection
  • in intraocular surgery
  • internally
  • if eye is lacerated or object is embedded
  • if seal is broken

Stop use and consult a doctor if you have

  • changes in vision
  • continued reddness, irritation or pain, or if the condition worsens or persists

Keep out of reach of children

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

Directions

Do not reuse.

Other information

Do not freeze

Inactive ingredients

benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

Questions?

Call 1-800-430-5490

Sperian Eye and Face Protection Inc

(a Honeywell Company)

825 East Highway 151

Platteville, WI 53818 USA

Package Label

EyeSalineConcentrate

EYESALINE CONCENTRATE 
water liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64809-104
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER92.2 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64809-104-182070 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/09/2011
2NDC:64809-104-195323 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/09/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34909/08/2011
Labeler - Sperian Eye & Face Protection Inc. (013435034)
Establishment
NameAddressID/FEIBusiness Operations
Sperian Eye & Face Protection Inc013435034manufacture(64809-104)

Revised: 3/2018
Document Id: 67eba057-1aa4-1604-e053-2991aa0a1d0b
Set id: b17d1415-e643-4f2f-b202-e46c6ec68d0c
Version: 8
Effective Time: 20180321
 
Sperian Eye & Face Protection Inc.