Harris Teeter Ultra Lubricant Eye Drops
- Manufacturer
- Harris Teeter, LLC. | K.C. Pharmaceuticals, Inc. | K.C. Pharmaceuticals, Inc
- Effective date
- 2024-01-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:58:24
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients
Polyethylene glycol 400......0.4%
Propylene glycol......0.3%
OTC - PURPOSE SECTION
Purpose
Polyethylene glycol 400......Lubricant
Propylene glycol......Lubricant
INDICATIONS & USAGE SECTION
Use
- 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 this product changes color or becomes cloudy
- if you are sensitive to any ingredient in this product
OTC - WHEN USING SECTION
When using this product
- do not touch tip of container to any surface to avoid contamination
- replace cap after each use
OTC - STOP USE SECTION
Stop use and ask a doctor if
- you feel eye pain
- changes in vision occur
- redness or irritation of the eye(s) gets worse or lasts more than 72 hours
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
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 or 2 drops in the affected eye(s) as needed
OTHER SAFETY INFORMATION
Other information
- Store at 15º-30°C (59°-86ºF)
INACTIVE INGREDIENT SECTION
Inactive ingredients
aminomethylpropanol, benzalkonium chloride as preservative, boric acid, hypromellose, potassium chloride, sorbitol
Harris Teeter Ultra Lubricant Eye Drops 15mL
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 477589 | polyethylene glycol 400, 0.4 % / propylene glycol 0.3 % Ophthalmic Solution | PSN | 1 |
| 477589 | polyethylene glycol 400 4 MG/ML / propylene glycol 3 MG/ML Ophthalmic Solution | SCD | 1 |
| 477589 | PEG 400 0.4 % / propylene glycol 0.3 % Ophthalmic Solution | SY | 1 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69256-980-01 | Harris Teeter Ultra Lubricant Eye Drops | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | 1 | |
| 69256-980-01 | Harris Teeter Ultra Lubricant Eye Drops | 1 in 1 BOX | SOLUTION/ DROPS | 1 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Harris Teeter Ultra Lubricant Eye Drops
- Polyethylene glycol 400, Propylene glycol
- AMINOMETHYLPROPANOL
- BENZALKONIUM CHLORIDE
- BORIC ACID
- HYPROMELLOSES
- POTASSIUM CHLORIDE
- WATER
- PROPYLENE GLYCOL
- SODIUM CHLORIDE
- SORBITOL
- POLYETHYLENE GLYCOL 400
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69256-980 | 69256-980-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| BORIC ACID | R57ZHV85D4 | IACT |
| HYPROMELLOSES | 3NXW29V3WO | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| WATER | 059QF0KO0R | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| SORBITOL | 506T60A25R | 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 |
|---|---|---|---|---|---|---|
| Harris Teeter Ultra Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Harris Teeter, LLC. | 31ac6883-ffc6-39de-e063-6294a90a52dd | 2024-01-01 | Warnings | 69256-980-01 69256-980 69256098001 31ac34cd-9f04-425f-e063-6394a90a04da 31ac6883-ffc6-39de-e063-6294a90a52dd |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
