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 if used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor’s instructions
Lubricant Eye Drops Preservative free 30 Single Use Container
- Manufacturer
- Nexus Optical Inc
- Effective date
- 2020-02-24
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:06:57
Label at a glance#
ProductLubricant Eye Drops Preservative free 30 Single Use Container
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure8 sections
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredients
Carboxymethylcellulose sodium 0.5%
Purposes
Lubricant
Use
- for the temporary relief of burning, irritation, and discomfort due to dryness of the eyes or exposure to wind or sun
- may be used as a protectant against further irritation
Warnings
For external use only
Do not use
- solution changes color or becomes cloudy
When using this product
- do not reuse
- once opened, discard
- to avoid contamination, do not touch tip of container to any surface
- do not touch unit-dose tip to eye
Stop use and ask a doctor if
- you experience eye pain
- changes in vision occur
- redness or irritation of the eye continues
- redness or irritation of the eye worsens or persists for more than 72 hours
Keep out of reach of children.
If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.
Directions
- to open, twist and pull tab to remove
- instill 1 or 2 drops in the affected eye(s) as needed and discard container
- if used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor’s instructions
Other information
- store at 15°-25°C (59°-77°F)
- use only if single-use container is intact
- use before expiration date marked on container
- RETAIN THIS CARTON FOR FUTURE REFERENCE
Inactive ingredients
calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride and sodium lactate. May contain sodium hydroxide and/or hydrochloric acid to adjust pH.
Questions or comments?
Call X-XXX-XXX-XXXX DAYS & TIMES & ZONE
Package Labeling:
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1188426 | carboxymethylcellulose sodium 0.5 % Ophthalmic Solution | PSN | 1 |
| 1188426 | carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution | SCD | 1 |
| 1188426 | carboxymethylcellulose sodium 0.5 % Ophthalmic Solution | SY | 1 |
| 1188426 | carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic Solution | SY | 1 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73450-002-05 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-bbe9-a426-e053-dadaa90af4c2 | Lubricant Eye Drops Preservative-free, 30 Single Use Container |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73450-002-05 | Lubricant Eye Drops Preservative free 30 Single Use Container | 30 in 1 BOX | LIQUID | 30 | 1 | |
| 73450-002-05 | Lubricant Eye Drops Preservative free 30 Single Use Container | 0.5 mL in 1 VIAL, SINGLE-USE | LIQUID | 0.5 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Lubricant Eye Drops Preservative free 30 Single Use Container
- CARBOXYMETHYLCELLULOSE SODIUM
- CALCIUM CHLORIDE
- MAGNESIUM CHLORIDE
- POTASSIUM CHLORIDE
- WATER
- SODIUM CHLORIDE
- SODIUM LACTATE
- CARBOXYMETHYLCELLULOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73450-002 | 73450-002-05 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CALCIUM CHLORIDE | M4I0D6VV5M | IACT |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| SODIUM LACTATE | TU7HW0W0QT | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM | K679OBS311 | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 9f57f9b5-e975-0365-e053-2a95a90adbbd | 9f57f9b5-e974-0365-e053-2a95a90adbbd | 2020-02-24 | Warnings | 9f57f9b5-e975-0365-e053-2a95a90adbbd 9f57f9b5-e974-0365-e053-2a95a90adbbd |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.