Indications and uses
For the temporarily relief of - burning and irritation due to dryness of the eye - redness of the eye due to minor eye irritation
See Clean-One Eye Drops
- Manufacturer
- Cho-A Pharm.Co.,Ltd.
- Effective date
- 2019-02-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:31:49
Label at a glance#
ProductSee Clean-One Eye Drops
Active ingredientBORIC ACID
Label structure8 sections
Dosage and administration
Instill 1-3 drops in the affected eye(s) 3-6 times a day
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient
Boric acid (1.546mg/1ml)
Purpose
Lubricant
Uses
For the temporarily relief of
- burning and irritation due to dryness of the eye
- redness of the eye due to minor eye irritation
Warnings
For external use only
Do not use
- if this product changes color or becomes cloudy
- if you are sensitive to any ingredient in this product
When using this product
- do not touch tip of container to any surface to avoid contamination
- remove contact lenses before using
- replace cap after use
Stop use and ask a doctor if
- you experience eye pain, changes in vision, continued redness or irritation of the eye
- conditions worsen
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
Instill 1-3 drops in the affected eye(s) 3-6 times a day
Inactive ingredients
Sulfamethoxazole, dipotassium glycyrrhizinate, Chlorpheniramine Maleate, Aminocaproic Acid, Disodium Edetate Hydrate, Sodium Tetraborate, Sodium hydroxide, Sterile Water for Injection
See Clean-One Eye Drops
Products#
Every source-derived product name is available through these pages.
- See Clean-One Eye Drops
- Boric acid
- SODIUM BORATE ANHYDROUS
- GLYCYRRHIZINATE DIPOTASSIUM
- EDETATE DISODIUM
- EDETIC ACID
- WATER
- CHLORPHENIRAMINE MALEATE
- AMINOCAPROIC ACID
- SODIUM HYDROXIDE
- SULFAMETHOXAZOLE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 58354-105 | 58354-105-01, 58354-105-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BORIC ACID | R57ZHV85D4 | ACTIB |
| SODIUM BORATE ANHYDROUS | 8191EN8ZMD | IACT |
| GLYCYRRHIZINATE DIPOTASSIUM | CA2Y0FE3FX | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| WATER | 059QF0KO0R | IACT |
| CHLORPHENIRAMINE MALEATE | V1Q0O9OJ9Z | IACT |
| AMINOCAPROIC ACID | U6F3787206 | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| SULFAMETHOXAZOLE | JE42381TNV | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 1b8d0870-302b-5f05-e063-6394a90a27f6 | 617a319f-05e1-46e6-e053-2a91aa0a8467 | 2024-06-23 | Warnings | 617a319f-05e1-46e6-e053-2a91aa0a8467 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.