CLEAR EYES NATURAL TEARS- polyvinyl alcohol and povidone liquid 
Prestige Brands Holdings, Inc.

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Clear Eyes Natural Tears

Drug Facts

Active ingredient

Polyvinyl alcohol 0.5%

Purpose

Lubricant

Active ingredient

Povidone 0.6%

Purpose

Lubricant

Uses

Warnings

For external use only.  

Do not use

if solution changes color or becomes cloudy.

When using this product

  • to avoid contamination, do not touch tip of container to any surface
  • replace cap after using

Stop use and ask a doctor if

  • you experience eye pain
  • you experience changes in vision
  • you experience continued redness or irritation of the eye
  • the condition worsens or symptoms last for more than 72 hours        

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Instill 1 to 2 drops in the affected eye(s) as needed.

Other information

Inactive ingredients

benzalkonium chloride, dextrose, edetate disodium, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate, sodium phosphate (mono- and dibasic)

Questions?

1-877-274-1787       Cleareyes.com 


PRINCIPAL DISPLAY PANEL

Clear eyes®

Natural Tears
Lubricant Eye Drops
STERILE 0.5 FL OZ (15 mL)

Clear eyes® 
Natural Tears
Lubricant Eye Drops 
STERILE 0.5 FL OZ (15 mL)

     

CLEAR EYES NATURAL TEARS 
polyvinyl alcohol and povidone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-557
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990) POLYVINYL ALCOHOL, UNSPECIFIED5.0 mg  in 1 mL
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE6.0 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
DEXTROSE (UNII: IY9XDZ35W2)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SODIUM PHOSPHATE (UNII: SE337SVY37)  
SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67172-557-021 in 1 BOX05/15/2013
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01805/15/2013
Labeler - Prestige Brands Holdings, Inc. (159655021)

Revised: 4/2024
Document Id: 95670119-5f19-4904-9123-759c88a54dc9
Set id: efba3eb0-798d-4635-b19b-4970e45b3cc9
Version: 10
Effective Time: 20240401
 
Prestige Brands Holdings, Inc.