Indications and 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.
REFRESH ® Classic ( P reservative-free ) Drug Facts
- Manufacturer
- Allergan, Inc.
- Effective date
- 2026-09-15
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 12
- Source
- daily-update
- Hydrated at
- 2026-09-25 02:01:48
Label at a glance#
ProductREFRESH Classic
Active ingredientPOLYVINYL ALCOHOL, UNSPECIFIED, Povidone
Label structure9 sections
Dosage and administration
To open, TWIST AND PULL TAB TO REMOVE . Instill 1 or 2 drops in the affected eye(s) as needed and discard container.
Label contents#
Full prescribing information#
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°-77°F (15°-25°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?
1.800.678.1605
refresheyedrops.com
v2.0DFL0506
Principal Display Panel
NDC 0023-0506-01
PRESERVATIVE-FREE
Refresh®
CLASSIC
Lubricant Eye Drops
Moisturizing Relief
For Dry, Irritated Eyes
30 Vials 0.01 fl oz (0.4 mL) each Sterile
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0023-0506-01 | EA - Each | 0023-0506 | 6f103f52-b51b-4112-8b6f-0dbff9ac462a | 1 | 2012-07-24 |
| 0023-0506-50 | EA - Each | 0023-0506 | d349c8e5-b120-43bc-a75d-eb0c165a554e | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Polyvinyl Alcohol | ACTIVE INGREDIENT | 532B59J990 | 4 | |
| Povidone | ACTIVE INGREDIENT | FZ989GH94E | 4 | |
| Polyvinyl Alcohol | ACTIVE MOIETY | 532B59J990 | 4 | |
| Povidone | ACTIVE MOIETY | FZ989GH94E | 4 | |
| hydrochloric acid | INACTIVE INGREDIENT | QTT17582CB | 4 | |
| sodium chloride | INACTIVE INGREDIENT | 451W47IQ8X | 4 | |
| sodium hydroxide | INACTIVE INGREDIENT | 55X04QC32I | 4 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | 4 |
Products#
Every source-derived product name is available through these pages.
- REFRESH Classic
- Polyvinyl Alcohol, Povidone
- POLYVINYL ALCOHOL, UNSPECIFIED
- Povidone
- water
- sodium chloride
- hydrochloric acid
- sodium hydroxide
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0023-0506 | 0023-0506-01, 0023-0506-50 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POLYVINYL ALCOHOL, UNSPECIFIED | 532B59J990 | ACTIB |
| Povidone | FZ989GH94E | ACTIB |
| water | 059QF0KO0R | IACT |
| sodium chloride | 451W47IQ8X | IACT |
| hydrochloric acid | QTT17582CB | IACT |
| sodium hydroxide | 55X04QC32I | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 11 | 2022-09-16 | full-release | 2026-06-01 01:58:03 |
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| hydrochloric acid | HYDROCHLORIC ACID | QTT17582CB | SOLUTION/ DROPS / OPHTHALMIC | ADJ PH | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION/ DROPS / OPHTHALMIC | ADJ PH | ||
| sodium chloride | SODIUM CHLORIDE | 451W47IQ8X | SOLUTION/ DROPS / OPHTHALMIC | 55 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION/ DROPS / OPHTHALMIC | ADJ PH | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION/ DROPS / OPHTHALMIC | ADJ PH | ||
| sodium chloride | SODIUM CHLORIDE | 451W47IQ8X | SOLUTION/ DROPS / OPHTHALMIC | 55 mg | ||
| hydrochloric acid | HYDROCHLORIC ACID | QTT17582CB | SOLUTION/ DROPS / OPHTHALMIC | ADJ PH | ||
| hydrochloric acid | HYDROCHLORIC ACID | QTT17582CB | SOLUTION/ DROPS / OPHTHALMIC | ADJ PH | ||
| sodium chloride | SODIUM CHLORIDE | 451W47IQ8X | SOLUTION/ DROPS / OPHTHALMIC | 55 mg |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 2481e2c0-dbd8-4cbf-a545-057c522b6b5c | 31bf1d6c-9719-4060-b6a3-409a2fe7b560 | 2022-09-16 | Warnings | 31bf1d6c-9719-4060-b6a3-409a2fe7b560 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.