Quality Choice Lubricant Eye Drops
- Manufacturer
- Chain Drug Marketing Assoc., Inc. | K.C. Pharmaceuticals, Inc. | Unimed Pharmaceuticals, Inc.
- Effective date
- 2023-12-23
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:17:14
Label at a glance#
ProductQuality Choice Lubricant Eye Drops
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure8 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients
Carboxymethylcellulose sodium.....0.5%
OTC - PURPOSE SECTION
Purpose
Lubricant
INDICATIONS & USAGE SECTION
Uses
- 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 SECTION
Warnings
For external use only
OTC - DO NOT USE SECTION
Do not use this product if
- solution changes color or becomes cloudy
OTC - WHEN USING SECTION
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
OTC - STOP USE SECTION
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
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of the 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, 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-operation (e.g., LASIK) dryness and discomfort, follow your eye doctor's instructions
OTHER SAFETY INFORMATION
Other information
- store at 15º-25ºC (59º-77ºF)
- use only if single-use container is intact
- use before expiration date marked on container
- RETAIN THIS CARTON FOR FUTURE REFERENCE
INACTIVE INGREDIENT SECTION
Inactive ingredients calcium chloride, **hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate.
**May contain these ingredients to adjust pH.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Quality Choice Lubricant Eye Drops
- carboxymethylcellulose sodium
- CALCIUM CHLORIDE
- HYDROCHLORIC ACID
- MAGNESIUM CHLORIDE
- POTASSIUM CHLORIDE
- SODIUM CHLORIDE
- WATER
- SODIUM HYDROXIDE
- CARBOXYMETHYLCELLULOSE
- SODIUM LACTATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63868-618 | 63868-618-30 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CALCIUM CHLORIDE | M4I0D6VV5M | IACT |
| HYDROCHLORIC ACID | QTT17582CB | IACT |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM | K679OBS311 | ACTIB |
| SODIUM LACTATE | TU7HW0W0QT | 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 |
|---|---|---|---|---|---|---|
| 213592bd-cfeb-6ecb-e063-6394a90ad43a | a0c78d11-3bbc-70c6-e053-2995a90a3ca8 | 2024-08-26 | Warnings | a0c78d11-3bbc-70c6-e053-2995a90a3ca8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.