Indications and uses
temporary relief of burning and irritation due to dryness of the eye as a protectant against further irritation temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun
temporary relief of burning and irritation due to dryness of the eye as a protectant against further irritation temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun
put 1 or 2 drops in the affected eye(s) as needed
store at room temperature discard 30 days
| Active ingredients | Purpose |
| Dextran 70 0.1% | Lubricant |
| Glycerin 0.2% | Lubricant |
| Hypromellose 0.3% | Lubricant |
For external use only
Stop use and ask a doctor if you experience any of the following:
If swallowed, get medical help or contact a Poison Control Center right away.
boric acid, calcium chloride, glycine, hydrochloric acid and/or sodium hydroxide (to adjust pH), magnesium chloride, polysorbate 80, potassium chloride, purified water, sodium chloride, zinc chloride. sodium borate, stabilized oxychloro complex
1-855-314-1850
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 70000-0588 | 70000-0588-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BORIC ACID | R57ZHV85D4 | IACT |
| CALCIUM CHLORIDE | M4I0D6VV5M | IACT |
| GLYCINE | TE7660XO1C | IACT |
| HYDROCHLORIC ACID | QTT17582CB | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
| POLIDRONIUM CHLORIDE | 6716Z5YR3G | IACT |
| POLYSORBATE 80 | 6OZP39ZG8H | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| ZINC CHLORIDE | 86Q357L16B | IACT |
| SODIUM BORATE | 91MBZ8H3QO | IACT |
| DEXTRAN 70 | 7SA290YK68 | ACTIB |
| GLYCERIN | PDC6A3C0OX | ACTIB |
| HYPROMELLOSES | 3NXW29V3WO | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 0fa82684-0906-5189-e063-6394a90aa7fc | d08ab451-e8d5-28bb-e053-2995a90a4c03 | 2024-01-23 | Warnings | d08ab451-e8d5-28bb-e053-2995a90a4c03 |
Adverse event summaries are temporarily unavailable. Other product information remains available.