Lubricant Eye Drops
- Manufacturer
- KC Pharmaceuticals, Inc.
- Effective date
- 2026-02-25
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:47:25
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Carboxymethylcellulose sodium 0.5%
OTC - PURPOSE SECTION
Eye Lubricant
INDICATIONS & USAGE SECTION
- 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
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.
DOSAGE & ADMINISTRATION SECTION
Directions
- To open, pull and twist tab to remove
- Instill 1 or 2 drops in the affected eye(s) as needed and discard container
INACTIVE INGREDIENT SECTION
Calcium Chloride, **Hydrochloric acid, Magnesium Chloride, Potassium Chloride, Purified water, Sodium Chloride, **Sodium Hydroxide, Sodium Lactate. **May contain these ingredients to adjust pH.
WARNINGS SECTION
Warnings
For external use only
Do not use this product if:
- 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 to eye
Stop use and ask a doctor if you experience any of the following
- you experience eye pain
- changes in vision occur
- redness or irritation of the eye continues
- redness or irritation of the eye gets worse or lasts more than 72 hours
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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 |
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0093351034121 | GTIN-13: 0093351034121 EAN-13: 0093351034121 GTIN-12: 093351034121 UPC-A: 093351034121 GTIN storage (14 digits): 00093351034121 | DiscountDrugMart_SDLP 5ct jpg.jpg |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55651-510-01 | Lubricant Eye Drops | 5 in 1 BOX | SOLUTION/ DROPS | 5 | 1 | |
| 55651-510-01 | Lubricant Eye Drops | 0.4 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 0.4 | 1 |
Products#
Every source-derived product name is available through these pages.
- Lubricant Eye Drops
- CARBOXYMETHYLCELLULOSE SODIUM
- WATER
- CALCIUM CHLORIDE
- CARBOXYMETHYLCELLULOSE
- MAGNESIUM CHLORIDE
- SODIUM CHLORIDE
- POTASSIUM CHLORIDE
- SODIUM HYDROXIDE
- SODIUM LACTATE
- HYDROCHLORIC ACID
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55651-510 | 55651-510-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| CALCIUM CHLORIDE | M4I0D6VV5M | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM | K679OBS311 | ACTIB |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| SODIUM LACTATE | TU7HW0W0QT | IACT |
| HYDROCHLORIC ACID | QTT17582CB | 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 |
|---|---|---|---|---|---|---|
| Lubricant Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM | KC Pharmaceuticals, Inc. | 4bafa882-50b7-e3e2-e063-6294a90a76e3 | 2026-02-25 | Warnings | 55651-510-01 55651-510 55651051001 4bafa893-cf6c-9e19-e063-6294a90a4f7e 4bafa882-50b7-e3e2-e063-6294a90a76e3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
