CARBOXYMETHYLCELLULOSE SODIUM 0.5% EYE LUBRICANT
- Manufacturer
- Cameron Pharmaceuticals
- Effective date
- 2026-04-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 01:53:44
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active Ingredient
Carboxymethylcellulose Sodium 0.5%
Purpose
Eye Lubricant
Use
- For the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to wind or sun.
- May be used as a protectant against further irritation.
Warnings
For use in the eyes only
- Retain outer carton for full product drug facts.
Do not use
- If solution changes color or becomes cloudy.
When using this product
- Avoid contamination, do not touch tip of container to any surface.
- Replace cap after use.
Stop use and ask a doctor if
- You experience eye pain, changes in vision, continued redness or irritationn of the eye.
- The condition worsens or persists for more than 72 hours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep this and all drugs out of the reach of children.If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Directions
- Shake well before use.
- Instill 1 or 2 drops in the affected eye(s) as needed.
Other information
- Store at room temperature 15°-30°C (59°- 86°F).
- Keep tightly closed.
Inactive ingredients
Boric acid, calcium chloride, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride. Stabilized Oxychloro Complex 2.5%. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.
Questions or comments?
1-888-767-7913
9am - 5pm EST
Monday - Friday
SPL UNCLASSIFIED SECTION
Distributed by: Cameron Pharmaceuticals, LLC
Louisville, KY 40245
PRINCIPAL DISPLAY PANEL - 2 Bottle Carton
TWIN PACK
CAMERON
PHARMACEUTICALS
™
Compare to Refresh Tears
®Lubricant
Eye Drops active ingredients
† †
NDC 42494-448-05
Lubricant
Eye Drops
CARBOXYMETHYLCELLULOSE SODIUM 0.5%
EYE LUBRICANT
MOISTURIZING
- Relieves burning, irritation
& discomfort due to dryness - For mild to moderate dry eye
- Sterile
2 Bottles
0.5 OZ (15 mL) Each
1.0 OZ (30 mL) TOTAL

DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1188426 | carboxymethylcellulose sodium 0.5 % Ophthalmic Solution | PSN | 4 |
| 1188426 | carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution | SCD | 4 |
| 1188426 | carboxymethylcellulose sodium 0.5 % Ophthalmic Solution | SY | 4 |
| 1188426 | carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic Solution | SY | 4 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 42494-448-05 | CARBOXYMETHYLCELLULOSE SODIUM EYE LUBRICANT | 15 mL in 1 BOTTLE, DISPENSING | SOLUTION/ DROPS | 15 | 4 | |
| 42494-448-05 | CARBOXYMETHYLCELLULOSE SODIUM EYE LUBRICANT | 2 in 1 CARTON | SOLUTION/ DROPS | 2 | 4 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 42494-448-05 | ML - Milliliter | 42494-448 | a0fb154a-bd76-4c3a-8e95-63aeba66380e | 1 | 2024-12-10 |
Products#
Every source-derived product name is available through these pages.
- CARBOXYMETHYLCELLULOSE SODIUM EYE LUBRICANT
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
- CALCIUM CHLORIDE
- MAGNESIUM CHLORIDE
- POTASSIUM CHLORIDE
- WATER
- SODIUM CHLORIDE
- SODIUM LACTATE
- HYDROCHLORIC ACID
- SODIUM HYDROXIDE
- CARBOXYMETHYLCELLULOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 42494-448 | 42494-448-05 |
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 |
| HYDROCHLORIC ACID | QTT17582CB | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED | 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 |
|---|---|---|---|---|---|---|
| 4f6fc835-bb2f-346c-e063-6394a90a9677 | dcff0759-aa56-49a0-9ea3-e64d96ee4328 | 2026-04-14 | Warnings | 4f6fc835-bb2f-346c-e063-6394a90a9677 dcff0759-aa56-49a0-9ea3-e64d96ee4328 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.