Indications and uses
for protection against further irritation for temporary relief of burning and irritation due to dryness of the eye
Foster and Thrive Dry Eye Relief
- Manufacturer
- Strategic Sourcing Services LLC | KC Pharmaceuticals, Inc.
- Effective date
- 2025-12-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 01:29:42
Label at a glance#
ProductFoster and Thrive Dry Eye Relief
Active ingredientPOLYETHYLENE GLYCOL 400
Label structure9 sections
Dosage and administration
instill 1 to 2 drops in the affected eye(s) as needed
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient
Polyethylene glycol 400 1%
Purpose
Lubricant
Uses
- for protection against further irritation
- for temporary relief of burning and irritation due to dryness of the eye
Warnings
For external use only
Do not use this product if
solution changes color or becomes cloudy
When using this product
- to avoid contamination, do not touch tip of container to any surface. Replace cap after using.
- remove contact lenses before using
Stop use and ask a 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
If pregnant or breast-feeding,
ask a health professional before use.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
instill 1 to 2 drops in the affected eye(s) as needed
Other information
store at 15°-30°C (59°-86°F)
Inactive ingredients
benzalkonium chloride, dextrose, edetate disodium, glycerin, hypromellose, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate, sodium phosphate dibasic, sodium phosphate monobasic
Questions or comments?
Call 833-358-6431
Monday to Friday
9:00am to 7:00pm EST
Foster & Thrive Dry Eye Relief 15mL
DailyMed RxNorm Mappings#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0010939958266 | GTIN-13: 0010939958266 EAN-13: 0010939958266 GTIN-12: 010939958266 UPC-A: 010939958266 GTIN storage (14 digits): 00010939958266 | Foster and Thrive Dry Eye Relief 15mL (revised).jpg |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70677-1157-1 | Foster and Thrive Dry Eye Relief | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | 4 | |
| 70677-1157-1 | Foster and Thrive Dry Eye Relief | 1 in 1 BOX | SOLUTION/ DROPS | 1 | 4 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70677-1157-1 | ML - Milliliter | 70677-1157 | 2298a8ac-8067-4522-a877-05aa605e54cf | 1 | 2024-03-12 |
Products#
Every source-derived product name is available through these pages.
- Foster and Thrive Dry Eye Relief
- Polyethylene glycol 400
- DEXTROSE
- WATER
- SODIUM PHOSPHATE, DIBASIC
- GLYCERIN
- HYPROMELLOSE, UNSPECIFIED
- SODIUM BICARBONATE
- SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS
- BENZALKONIUM CHLORIDE
- EDETATE DISODIUM
- POTASSIUM CHLORIDE
- SODIUM CHLORIDE
- SODIUM CITRATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70677-1157 | 70677-1157-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| Foster and Thrive Dry Eye Relief | POLYETHYLENE GLYCOL 400 | Strategic Sourcing Services LLC | 0018ade9-5856-db6c-e063-6394a90a2ccf | 2025-12-30 | Warnings | 70677-1157-1 70677-1157 70677115701 4749275b-6982-4eaf-e063-6394a90aaee9 0018ade9-5856-db6c-e063-6394a90a2ccf |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.