Indications and uses
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.
Carboxymethylcellulose Sodium 0.5% Lubricant Eye Drops
- Manufacturer
- Golden State Medical Supply, Inc. | Huons Co., Ltd.
- Effective date
- 2025-02-25
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:55:52
Label at a glance#
ProductCarboxymethylcellulose Sodium 0.5%
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure10 sections
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. Follow your eye doctor’s instructions if you are using this product after an eye surgery (e.g., LASIK) to relieve eye dryness and discomfort.
Contacts and useful links#
Websitewww.gsms.us
www.gsms.us
www.gsms.usLabel contents#
Full prescribing information#
Active Ingredients
Carboxymethylcellulose sodium 0.5%
Purpose
Eye lubricant
Uses
- 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 external use only.
- To avoid contamination, do not touch tip of container to any surface.
- Do not reuse. Once opened, discard.
- Do not touch unit-dose tip to eye.
Do not use
If solution changes color or becomes cloudy.
Stop use and ask a doctor if
you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- To open, TWIST AND PULL TAB TO REMOVE. Instill 1 or 2 drops in the affected eye(s) as needed and discard container.
- Follow your eye doctor’s instructions if you are using this product after an eye surgery (e.g., LASIK) to relieve eye dryness and discomfort.
Other information
- Use only if single-use container is intact.
- Use before expiration date marked on container.
- Store at 59°-77°F (15°-25°C).
- RETAIN THIS CARTON FOR FUTURE REFERENCE.
Inactive ingredients
Calcium chloride dihydrate; magnesium chloride hexahydrate; potassium chloride; purified water; sodium chloride; and sodium lactate. May contain hydrochloric acid and/or sodium hydroxide (to adjust pH).
Questions or comments?
Call 1 (800) 284-8633, Monday to Friday 7 AM-4PM PST or visit www.gsms.us
TAMPER EVIDENT
DO NOT USE THIS PRODUCT IF THE INNER POUCH IS OPEN, TORN, OR MISSING.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Carton
Preservative free
NDC 51407-945-30
Carboxymethylcellulose
Sodium
0.5%
Lubricant Eye Drops
Sterile
30 Single-Use Containers
0.02 FL OZ (0.5 mL) each
gsms
Manufactured by:
Huons Co,, Ltd.
Jecheon-si, Chungcheongbuk-do,
27159. South Korea
Marketed by:
GSMS Incorporated
Camarillo, CA 93012 USA
Rev. 01/25
Pouch
Preservative free
Carboxymethylcellulose
Sodium
Lubricant Eye Drops
0.5 mL
Single-Use
gsms
Open along the dotted line.
Label
Carboxymethylcellulose Sodium
Eye Drops Single-Use 0.5 mL
gsms
Rev. 01/25
EL9044-00
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#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51407-945-30 | Carboxymethylcellulose Sodium 0.5% | 3 in 1 CARTON | SOLUTION/ DROPS | 3 | 1 | |
| 51407-945-30 | Carboxymethylcellulose Sodium 0.5% | 10 in 1 POUCH | SOLUTION/ DROPS | 10 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51407-945-30 | EA - Each | 51407-945 | a5c710bd-b3c4-4132-9245-6b19341bdeb3 | 1 | 2025-05-14 |
Products#
Every source-derived product name is available through these pages.
- Carboxymethylcellulose Sodium 0.5%
- HYDROCHLORIC ACID
- SODIUM CHLORIDE
- CARBOXYMETHYLCELLULOSE SODIUM
- CARBOXYMETHYLCELLULOSE
- CALCIUM CHLORIDE
- SODIUM LACTATE
- SODIUM HYDROXIDE
- MAGNESIUM CHLORIDE
- POTASSIUM CHLORIDE
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51407-945 | 51407-945-30 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYDROCHLORIC ACID | QTT17582CB | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM | K679OBS311 | ACTIB |
| CALCIUM CHLORIDE | M4I0D6VV5M | IACT |
| SODIUM LACTATE | TU7HW0W0QT | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| 2e8a5fe2-144b-cdbb-e063-6394a90a2835 | 2e8a5fe2-144a-cdbb-e063-6394a90a2835 | 2025-02-25 | Warnings | 2e8a5fe2-144b-cdbb-e063-6394a90a2835 2e8a5fe2-144a-cdbb-e063-6394a90a2835 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.