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.
Moderate lubricating drops
- Manufacturer
- Velocity Pharma LLC
- Effective date
- 2022-06-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:58:49
Label at a glance#
ProductModerate lubricating drops CVS Health
Active ingredientPOLYETHYLENE GLYCOL 400
Label structure10 sections
Dosage and administration
Instill 1 or 2 drops in the affected eye(s) as needed.
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Polyethylene Glycol 400 0.25%
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. Replace cap after using.
- Do not use if solution changes color or becomes cloudy.
Stop use and ask 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 - KEEP OUT OF REACH OF CHILDREN SECTION
If swallowed, get medical help of contact a Poison Control Center right away.
Directions
Instill 1 or 2 drops in the affected eye(s) as needed.
Other Information
Discard 30 days after opening
RETAIN THIS CARTON FOR FUTURE REFERENCE.
INACTIVE INGREDIENT SECTION
Boric acid, calcium chloride, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium chlorite (OcuPure ® Brand) as a preservative; Sodium Hyaluronate.
Principal Display Panel - 15 mL Bottle Carton
Products#
Every source-derived product name is available through these pages.
- Moderate lubricating drops CVS Health
- polyethylene glycol 400
- BORIC ACID
- CALCIUM CHLORIDE
- MAGNESIUM CHLORIDE
- POTASSIUM CHLORIDE
- WATER
- SODIUM BORATE
- SODIUM CHLORIDE
- SODIUM CHLORITE
- HYALURONATE SODIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 76168-711 | 76168-711-15 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BORIC ACID | R57ZHV85D4 | IACT |
| CALCIUM CHLORIDE | M4I0D6VV5M | IACT |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM BORATE | 91MBZ8H3QO | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| SODIUM CHLORITE | G538EBV4VF | IACT |
| HYALURONATE SODIUM | YSE9PPT4TH | IACT |
| POLYETHYLENE GLYCOL 400 | B697894SGQ | 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 |
|---|---|---|---|---|---|---|
| 0fa853a8-61a8-5e6d-e063-6294a90a38ee | e2016198-48ce-9cbc-e053-2995a90ac47d | 2024-01-23 | Warnings | e2016198-48ce-9cbc-e053-2995a90ac47d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.