GNP Eye Drops Redness & Dry Eye Relief (PLD)
- Manufacturer
- AmerisourceBergen | K.C. Pharmaceuticals, Inc.
- Effective date
- 2026-06-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- daily-update
- Hydrated at
- 2026-07-15 00:32:52
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients
Glycerin.....0.25%
Naphazoline HCl.....0.012%
OTC - PURPOSE SECTION
Purposes
Glycerin.....Lubricant
Naphazoline HCl.....Redness reliever
INDICATIONS & USAGE SECTION
Uses
- relieves redness of eye due to minor eye irritations
- for use as a protectant against further irritation or to relieve dryness of the eye
- for the temporary relief of burning and irritation due to dryness of the eye
WARNINGS SECTION
Warnings
For external use only
OTC - DO NOT USE SECTION
Do not use if solution changes color or becomes cloudy
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have narrow angle glaucoma
OTC - WHEN USING SECTION
When using this product
- to avoid contamination, do not touch tip of container to any surface
- replace cap after using
- overuse may produce increased redness of the eye
- pupils may become enlarged temporarily
OTC - STOP USE SECTION
Stop use and ask a doctor if
- you experience eye pain
- you experience changes in vision
- you experience continued redness or irritation of the eye
- the condition worsens or persists for more than 72 hours
OTC - STOP USE SECTION
Stop use and ask a doctor if
- you experience eye pain
- you experience changes in vision
- you experience 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.
DOSAGE & ADMINISTRATION SECTION
Directions
Instill 1 to 2 drops in the affected eye(s) up to 4 times daily.
OTHER SAFETY INFORMATION
Other information
store at room temperature
INACTIVE INGREDIENT SECTION
Inactive ingredients
benzalkonium chloride, boric acid, edetate disodium, purified water, sodium borate
OTC - QUESTIONS SECTION
Questions or comments?
Call 1-800-527-4276
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0087701432026 | GTIN-13: 0087701432026 EAN-13: 0087701432026 GTIN-12: 087701432026 UPC-A: 087701432026 GTIN storage (14 digits): 00087701432026 | GNPEyeDr RednDryEye Rel.jpg |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 777d68c6-a5ab-e06c-d314-677b0b9af0c8 | Product name | 2 | 20240508 |
| e18001c8-33ae-5f66-9cdc-a39724bd4573 | Product name | 1 | 20140508 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 46122-606-05 | ML - Milliliter | 46122-606 | cf8edbce-cdff-4830-a744-bec97b88ae8d | 1 | 2023-02-06 |
Products#
Every source-derived product name is available through these pages.
- GNP Eye Drops Redness and Dry Eye Relief
- glycerin, naphazoline HCl
- BENZALKONIUM CHLORIDE
- EDETATE DISODIUM
- EDETIC ACID
- WATER
- SODIUM BORATE
- BORIC ACID
- GLYCERIN
- NAPHAZOLINE HYDROCHLORIDE
- NAPHAZOLINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 46122-606 | 46122-606-05 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM BORATE | 91MBZ8H3QO | IACT |
| BORIC ACID | R57ZHV85D4 | IACT |
| GLYCERIN | PDC6A3C0OX | ACTIB |
| NAPHAZOLINE HYDROCHLORIDE | MZ1131787D | ACTIB |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 3 | 2023-12-23 | full-release | 2026-06-01 00:05:36 |
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 |
|---|---|---|---|---|---|---|
| 546a55db-3cbf-9962-e063-6294a90aebd9 | 9b5c8b83-36c5-765b-e053-2995a90a395c | 2026-06-16 | Warnings | 546a55db-3cbf-9962-e063-6294a90aebd9 9b5c8b83-36c5-765b-e053-2995a90a395c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
