Storage and handling
Other information Use only if single-use container is intact Use before expiration date marked on container Store at 59°-86°F (15°-33°C) RETAIN THIS CARTON FOR FUTURE REFERENCE
Real Lubricant Eye Drops
- Manufacturer
- Oliver Landon Intl Inc.
- Effective date
- 2021-12-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:45:26
Label at a glance#
ProductReal
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure10 sections
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Carboxymethylcellulose sodium 0.5%
OTC - PURPOSE SECTION
Purpose
Eye Lubricant
INDICATIONS & USAGE SECTION
Use
- For 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 SECTION
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
- If solution changes color or becomes cloudy, do not use
OTC - STOP USE SECTION
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.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a doctor before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
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 dryness and discomfort, follow your eye doctor’s instructions.
STORAGE AND HANDLING SECTION
Other information
- Use only if single-use container is intact
- Use before expiration date marked on container
- Store at 59°-86°F (15°-33°C)
- RETAIN THIS CARTON FOR FUTURE REFERENCE
INACTIVE INGREDIENT SECTION
Inactive ingredients Calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride and sodium lactate. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.
Questions or Comments?
info@oliverlandon.biz
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 59276-403-05
Real
Lubricant Eye Drops
- Moisturizing relief
- Immediate, soothing relief for dry eyes.
Preservative-free
Directions
To open, TWIST AND PULL TAB TO REMOVE
Instill 1 or 2 drops in the affected eye(s) as needed and discard container.
5 Single-Use Containers
0.01 fl oz (0.4 mL) each Sterile
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1188426 | carboxymethylcellulose sodium 0.5 % Ophthalmic Solution | PSN | 2 |
| 1188426 | carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution | SCD | 2 |
| 1188426 | carboxymethylcellulose sodium 0.5 % Ophthalmic Solution | SY | 2 |
| 1188426 | carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic Solution | SY | 2 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 59276-403-05 | 2024-01-30 | C162847 | 48780-1 | 1030e365-4db2-111a-e063-dadaa90a10e2 | Real Lubricant Eye Drops |
| 59276-403-30 | 2024-01-30 | C162847 | 48780-1 | 1030e365-4db2-111a-e063-dadaa90a10e2 | Real Lubricant Eye Drops |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59276-403-05 | Real | 0.4 mL in 1 VIAL, SINGLE-USE | SOLUTION/ DROPS | 0.4 | 2 | |
| 59276-403-05 | Real | 5 in 1 CARTON | SOLUTION/ DROPS | 5 | 2 | |
| 59276-403-30 | Real | 0.4 mL in 1 VIAL, SINGLE-USE | SOLUTION/ DROPS | 0.4 | 2 | |
| 59276-403-30 | Real | 30 in 1 CARTON | SOLUTION/ DROPS | 30 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Real
- carboxymethylcellulose sodium
- CALCIUM CHLORIDE
- MAGNESIUM CHLORIDE
- POTASSIUM CHLORIDE
- WATER
- SODIUM CHLORIDE
- SODIUM LACTATE
- HYDROCHLORIC ACID
- SODIUM HYDROXIDE
- CARBOXYMETHYLCELLULOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 59276-403 | 59276-403-05, 59276-403-30 |
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 | 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 |
|---|---|---|---|---|---|---|
| b4e02102-512d-4113-e053-2995a90a2efd | 580474a2-d640-49cf-b50c-c83420e52e1a | 2021-12-05 | Warnings | b4e02102-512d-4113-e053-2995a90a2efd 580474a2-d640-49cf-b50c-c83420e52e1a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.