Skip to Content

Clear Eyes Natural Tears

Medically reviewed on May 22, 2017.

Dosage form: liquid
Ingredients: POLYVINYL ALCOHOL, UNSPECIFIED 5.0mg in 1mL, POVIDONE 6.0mg in 1mL
Labeler: Prestige Brands Holdings, Inc.
NDC Code: 67172-557

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.

Clear Eyes Natural Tears

Drug Facts

Active ingredient

Polyvinyl alcohol 0.5%

Purpose

Lubricant

Active ingredient

Povidone 0.6%

Purpose

Lubricant

Uses
  • for the temporary relief of burning and irritation due to dryness of the eye
  • for use as a protectant against further irritation or to relieve dryness of the eye 

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
  • symptoms lasts 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
  • store at room temperature
  • remove contact lenses before using

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       www.cleareyes.com 


PRINCIPAL DISPLAY PANEL

Clear eyes® Natural Tears
Lubricating 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 AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYVINYL ALCOHOL, UNSPECIFIED (POLYVINYL ALCOHOL, UNSPECIFIED) POLYVINYL ALCOHOL, UNSPECIFIED5.0 mg  in 1 mL
POVIDONE (POVIDONE) POVIDONE6.0 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE 
DEXTROSE 
EDETATE DISODIUM 
POTASSIUM CHLORIDE 
WATER 
SODIUM BICARBONATE 
SODIUM CHLORIDE 
SODIUM CITRATE 
SODIUM PHOSPHATE 
Packaging
#Item CodePackage Description
1NDC:67172-557-021 BOTTLE, DROPPER in 1 BOX
115 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34905/15/2013
Labeler - Prestige Brands Holdings, Inc. (159655021)

 
Prestige Brands Holdings, Inc.

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.

Hide