Indications and uses
● relieves dryness of the eye(s). ● for the temporary relief of discomfort due to minor irritations of the eye from exposure to wind or sun. ● as a protectant against further irritation.
● relieves dryness of the eye(s). ● for the temporary relief of discomfort due to minor irritations of the eye from exposure to wind or sun. ● as a protectant against further irritation.
● Instill 1or 2 drops into the affected eye(s) as needed.
EQUATE COMFORT GEL
49035-197-49
Drug Facts
Carboxymethylcellulose Sodium 0.25%
Hypromellose 0.3%
Eye Lubricant
Eye Lubricant
● relieves dryness of the eye(s).
● for the temporary relief of discomfort due to minor irritations of the eye from exposure to wind or sun.
● as a protectant against further irritation.
For use in the eyes only.
● Retain outer carton for full product drug facts.
● if this product changes color or becomes cloudy.
● avoid contamination, do not touch tip of container to any surface.
● replace cap after each use.
● you experience eye pain, changes in vision, continued redness or irritation of the eye(s).
● the condition worsens or persists for more than 72 hours.
If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222).
● Instill 1or 2 drops into the affected eye(s) as needed.
● store at room temperature 15º-30ºC (59º-86ºF).
● keep tightly closed.
Boric acid, calcium chloride, citric acid, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride. Vanish® (Stabilized Peroxycomplex System as a preservative). May also contain hydrochloric acid and or sodium hydroxide to adjust pH.
1-888-287-1915
NDC 49035-197-49
equate
Comfort Gel
LUBRICANT EYE GEL
CARBOXYMETHYCELLULOSE SODIUM 0.25%
HYPROMELLOSE 0.3%
Sterile
2- 0.5 FL OZ (15mL) BOTTLES
1 FL OZ (30mL) TOTAL
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49035-197-49 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-105d-f424-e053-dadaa90a57ce | Equate Comfort Gel |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 49035-197 | 49035-197-49 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYPROMELLOSES | 3NXW29V3WO | ACTIB |
| CARBOXYMETHYLCELLULOSE SODIUM | K679OBS311 | ACTIB |
| BORIC ACID | R57ZHV85D4 | IACT |
| CALCIUM CHLORIDE | M4I0D6VV5M | IACT |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM BORATE | 91MBZ8H3QO | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| CHLORINE DIOXIDE | 8061YMS4RM | IACT |
| POLIHEXANIDE | 322U039GMF | IACT |
| HYDROCHLORIC ACID | QTT17582CB | CNTM |
| SODIUM HYDROXIDE | 55X04QC32I | CNTM |
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 |
|---|---|---|---|---|---|---|
| 2755662a-389d-4553-844b-97f0a35bd603 | d1b915ea-c860-4daf-9e88-41f17128a7ce | 2018-01-19 | Warnings | 2755662a-389d-4553-844b-97f0a35bd603 d1b915ea-c860-4daf-9e88-41f17128a7ce |
Adverse event summaries are temporarily unavailable. Other product information remains available.