Indications and uses
For relief of dryness of the eye, and protectant against further irritation of the eye. For temporary relief of buming, irritation, and discomfort including exposure to wind or sun.
Walgreens Lubricant Eye Drops
- Manufacturer
- WALGREEN COMPANY
- Effective date
- 2023-05-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:31:48
Label at a glance#
ProductWalgreens Lubricant Eye Drops
Active ingredientPROPYLENE GLYCOL
Label structure8 sections
Dosage and administration
• Shake well. • Wash your hands. • Instill 1 or 2 drops in the affected eye(s) as needed.
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
| Active Ingredients | Purpose |
| Propylene Glycol 0.6% | Lubricant |
OTC - PURPOSE SECTION
Uses
- For relief of dryness of the eye, and protectant against further irritation of the eye.
- For temporary relief of buming, irritation, and discomfort including exposure to wind or sun.
Warnings
• For use in eyes only.
• For external use only.
• Retain outer carton for full product drug facts.
• To avoid contamination, do not touch tip of container to any surface. Close cap after using.
• If solution changes color or becomes cloudy, do not use.
When using this product
• Retain outer carton for full product drug facts.
• To avoid contamination, do not touch tip of container to any surface. Close cap after using.
• If solution changes color or becomes cloudy, do not use.
OTC - STOP USE SECTION
Stop use and ask a doctor if you experience any of the following:
• You experience eye pain, changes in vision, continued redness or irritation of the eye.
• The condition worsens or persists for more than 72 hours.
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 (1-800-222-1222) right away.
Pregnancy or Breast Feeding
• If pregnant or breast feeding, ask a health professional before use.
Directions
• Shake well.
• Wash your hands.
• Instill 1 or 2 drops in the affected eye(s) as needed.
Other Information
• Use only if imprinted tape seals on top and bottom flaps are intact and clearly legible.
• Use before expiration date marked on container. • Discard 30 days after opening.
• Store at 59°-86° F (15°-30°C).
Inactive Ingredients
Highly purified water, Boric acid, Hypromellose, Sodium borate, Sodium chloride, Calcium chloride, Benzalkonium chloride, Potassium chloride, Disodium edetate, Magnesium chloride, HCI to adjust pH.
Questions or Comments?
1-800-925-4733
9 am to 5 pm EST;
Monday - Friday.
PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0363-2112-15 | 2025-12-23 | C162847 | 48780-1 | 1e7a6dab-1b7b-a2ce-e063-dadaa90aadf7 | Walgreens Lubricant Eye Drops (Systane COMPLETE) Drug Facts |
| 0363-2112-15 | 2024-07-30 | C162847 | 48780-1 | 1e7a6dab-1b7b-a2ce-e063-dadaa90aadf7 | Walgreens Lubricant Eye Drops (Systane COMPLETE) Drug Facts |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Walgreens Lubricant Eye Drops
- propylene glycol
- BORIC ACID
- EDETATE DISODIUM
- HYPROMELLOSES
- CALCIUM CHLORIDE
- WATER
- HYDROCHLORIC ACID
- MAGNESIUM CHLORIDE
- SODIUM BORATE
- BENZALKONIUM CHLORIDE
- SODIUM CHLORIDE
- POTASSIUM CHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0363-2112 | 0363-2112-15 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BORIC ACID | R57ZHV85D4 | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| HYPROMELLOSES | 3NXW29V3WO | IACT |
| CALCIUM CHLORIDE | M4I0D6VV5M | IACT |
| WATER | 059QF0KO0R | IACT |
| HYDROCHLORIC ACID | QTT17582CB | IACT |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
| SODIUM BORATE | 91MBZ8H3QO | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | ACTIB |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | 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 |
|---|---|---|---|---|---|---|
| 43d83f90-7f66-17d2-e063-6394a90a53b2 | f308798d-7df3-420a-e053-2995a90a76b6 | 2025-11-17 | Warnings | f308798d-7df3-420a-e053-2995a90a76b6 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.