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REFRESH Classic by Allergan, Inc.

Medically reviewed on April 27, 2018

Dosage form: solution/ drops
Ingredients: Polyvinyl Alcohol 14mg in 1mL, Povidone 6mg in 1mL
Labeler: Allergan, Inc.
NDC Code: 0023-0506

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.

REFRESH Classic

Drug Facts

Active ingredients

Polyvinyl Alcohol 1.4%

Povidone 0.6%

Purpose

Eye lubricant

Eye lubricant

Uses
  • For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun.
  • May be used as a protectant against further irritation.

Warnings
  • For external use only.
  • To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.
  • Do not touch unit-dose tip to eye.
  • If solution changes color or becomes cloudy, do not use.

Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

To open, TWIST AND PULL TAB TO REMOVE. Instill 1 or 2 drops in the affected eye(s) as needed and discard container.

Other information
  • Use only if single-use container is intact.
  • Use before expiration date marked on container.
  • Store at 59°-86°F (15°-30°C).
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Purified water and sodium chloride. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions or comments?

1.800.433.8871

refreshbrand.com

NDC 0023-0506-01

Preservative-free

Refresh®
Classic
Lubricant Eye Drops

Moisture drops
for dry eyes

30 Single-Use Containers
0.01 fl oz (0.4 mL) each Sterile

REFRESH CLASSIC 
polyvinyl alcohol, povidone solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-0506
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Polyvinyl Alcohol (Polyvinyl Alcohol) Polyvinyl Alcohol14 mg  in 1 mL
Povidone (Povidone) Povidone6 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
sodium chloride 
hydrochloric acid 
sodium hydroxide 
Packaging
#Item CodePackage Description
1NDC:0023-0506-0130 VIAL, SINGLE-USE in 1 CARTON
10.4 mL in 1 VIAL, SINGLE-USE
2NDC:0023-0506-5050 VIAL, SINGLE-USE in 1 CARTON
20.4 mL in 1 VIAL, SINGLE-USE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34909/12/1985
Labeler - Allergan, Inc. (144796497)
Establishment
NameAddressID/FEIOperations
Allergan Sales, LLC362898611MANUFACTURE(0023-0506)
Establishment
NameAddressID/FEIOperations
Allergan Pharmaceuticals Ireland219682291MANUFACTURE(0023-0506)

 
Allergan, Inc.

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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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