Indications and uses
for use as a protectant against further irritation or to relieve dryness of the eye for the temporary relief of discomfort due to minor irritations of the eye, or to exposure to wind or sun
for use as a protectant against further irritation or to relieve dryness of the eye for the temporary relief of discomfort due to minor irritations of the eye, or to exposure to wind or sun
Instill 1 or 2 drops in the affected eye(s) as needed.
Tamper Evident. Do not use this product if neckband is missing or broken. RETAIN THIS CARTON FOR FUTURE REFERENCE Store at 15°-30°C (59°-86°F)
Carboxymethylcellulose Sodium 10 MG in 1 ml.
Eye Lubricant
For external use only
• Do not use this product if solution changes color or becomes cloudy
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
When using this product
• to avoid contamination. do not touch tip of container to any surface • replace cap after using. Keep container tightly closed.
• remove contact lens before using
Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center immediately.
Instill 1 or 2 drops in the affected eye(s) as needed.
Boric Acid
Potassium Chloride
Sodium Chloride
Calcium Chloride Dihydrate.
Magnesium Chloride
Sodium Chlorite
Sodium Hydroxide and Water for Injection
1-866-826-1306
between 9 am and 4 pm EST, Monday-Friday.
Compare to the active Ingredient in Refresh Plus Eye Drops
Carboxymethylcellulose Sodium 1%
Lubricant Eye Drops
Refresh, Lubricate and Moisturizes
Distributed by:
Delsam Pharma Llc
Bronx, Newyork 10467.
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72570-121-15 | ML - Milliliter | 72570-121 | 5112ebaf-5eb8-4703-b8b6-7e5da32228bc | 1 | 2021-06-02 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 72570-121 | 72570-121-15 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED | K679OBS311 | ACTIB |
| BORIC ACID | R57ZHV85D4 | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| CALCIUM CHLORIDE | M4I0D6VV5M | IACT |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
| SODIUM CHLORITE | G538EBV4VF | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| WATER | 059QF0KO0R | IACT |
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 |
|---|---|---|---|---|---|---|
| e7c36253-3970-4ed6-bdc3-cc4439be2f02 | fbbfda9c-588b-4e82-b66c-83cea663b967 | 2023-03-15 | Warnings | fbbfda9c-588b-4e82-b66c-83cea663b967 |
Adverse event summaries are temporarily unavailable. Other product information remains available.