Quick answers
- What is Polyethylene glycol 400 used for?
- The Drug Facts label of Blink Triple Care Preservative Free (Bausch & Lomb Incorporated) lists these uses: for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun for use as a protectant against further irritation or to relieve dryness of the eye for use as a lubricant to prevent further irritation or to relieve dryness of the eye.
- Do I need a prescription for Polyethylene glycol 400?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredient, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Polyethylene glycol 400 been recalled?
- FDA enforcement reports list 1 recall of products on this page; the newest started September 11, 2026. A recall usually concerns specific products or lots, not every brand.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Blink Triple Care Preservative Free · Bausch & Lomb Incorporated
Polyethylene glycol 400 2.5 mg/mL, solution/ drops (ophthalmic)
Active ingredient
Polyethylene glycol 400 0.25%
Purpose
Lubricant
Uses
for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun for use as a protectant against further irritation or to relieve dryness of the eye for use as a lubricant to prevent further irritation or to relieve dryness of the eye
Warnings
For external use only
Do not use
if product changes color
When using this product
to avoid contamination, do not touch tip of container to any surface replace cap after each use
Stop use and ask a doctor if
you experience eye pain, changes in vision, continued redness or irritation of the eye condition worsens or persists for more than 72 hours Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
shake well before use. instill 1 or 2 drops in the affected eye(s) as needed or as directed by your eye care professional.
Inactive ingredients
boric acid, castor oil, polyoxyl-40 hydrogenated castor oil. potassium chloride, purified water, sodium borate, sodium chloride, sodium hyaluronate.
Questions?
[phone icon] Call: 1-800-553-5340
— FDA label of Blink Triple Care Preservative Free, Bausch & Lomb Incorporated, effective May 27, 2026. See the official label on DailyMed →
Visine Dry Eye Relief Eye Drops · Kenvue Brands LLC
Polyethylene glycol 400 10 mg/mL, solution/ drops (ophthalmic)
Active ingredient
Polyethylene glycol 400 1%
Purpose
Lubricant
Uses
for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun for protection against further irritation
Warnings
For external use only
When using this product
remove contact lenses before using do not use if this solution changes color or becomes cloudy do not touch tip of container to any surface to avoid contamination replace cap after each use
Stop use and ask a doctor if
you feel eye pain changes in vision occur redness or irritation of the eye lasts condition worsens or lasts 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 right away.
Directions
adults and children 6 years of age and over: put 1 or 2 drops in the affected eye(s) as needed children under 6 years of age: consult a doctor
Inactive ingredients
ascorbic acid, boric acid, dextrose, glycerin, glycine, hypromellose, magnesium chloride, polyquaternium-42, potassium chloride, purified water, sodium borate, sodium chloride, sodium citrate, sodium lactate, sodium phosphate dibasic
Questions?
call toll-free 888-734-7648 or 215-273-8755 (collect)
— FDA label of Visine Dry Eye Relief Eye Drops, Kenvue Brands LLC, effective November 13, 2024. See the official label on DailyMed →
Foster and Thrive Dry Eye Relief · Strategic Sourcing Services LLC
Polyethylene glycol 400 1%, solution/ drops (ophthalmic)
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?
Call 833-358-6431 Monday to Friday 9:00am to 7:00pm EST
— FDA label of Foster and Thrive Dry Eye Relief, Strategic Sourcing Services LLC, effective December 30, 2025. See the official label on DailyMed →
Dr.Harry EYES PROTECTION · Wenzhou Yuyuan Pharmaceutical Co., Ltd.
Polyethylene glycol 400 1%, spray (topical)
Active ingredient
Polyethylene glycol 400 1%
Purpose
Lubricant
Uses
Refreshes eye contour,delivers fresh sensation, hydrates and maintains eye skin moisture for instant refreshing comfort.
Warnings
For external use only.
Do not use
if solution changes color or becomes cloudy Ask Doctor Discontinue use if irritation appears. Seek medical help for eye stinging, itching or blurred vision. When Using If pregnant or breast‑feeding,ask a health professional before use. Do not swallow. Avoid eye contact; rinse well with water if contact occurs. Stop Use Discontinue use if irritation appears. Seek medical help for eye stinging, itching or blurred vision. Keep Out Of Reach Of Children Keep away from children & pets.
Directions
Spray 1‑2 times onto closed eyelids from about 10cm away,up to 4 times daily.
Inactive ingredients
Calendula Officinalis Flower Extract,Lutein,Hydrolyzed Sodium Hyaluronate, Purified Water,Vitamin B5,Vitamin A Palmitate, Vitamin E,Glycerin,Butylene Glycol,Ethylhexylglycerin.
— FDA label of Dr.Harry EYES PROTECTION, Wenzhou Yuyuan Pharmaceutical Co., Ltd., effective September 3, 2026. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredient, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Polyethylene glycol 400 2.5 mg/mL · solution/ drops (ophthalmic) · 5 products
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Blink Gel Tears | Bausch & Lomb Incorporated | DailyMed |
| Blink Tears | Bausch & Lomb Incorporated | DailyMed |
| Blink Triple Care | Bausch & Lomb Incorporated | DailyMed |
| Blink Triple Care Preservative Free | Bausch & Lomb Incorporated | DailyMed |
Polyethylene glycol 400 10 mg/mL · solution/ drops (ophthalmic) · 3 products
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Visine Dry Eye Relief | Kenvue Brands LLC | DailyMed |
| Visine Dry Eye Relief Eye Drops | Kenvue Brands LLC | DailyMed |
Polyethylene glycol 400 1% · solution/ drops (ophthalmic) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Foster and Thrive Dry Eye Relief | Strategic Sourcing Services LLC | DailyMed |
Polyethylene glycol 400 1% · spray (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Dr.Harry EYES PROTECTION | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | DailyMed |
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Bausch & Lomb Incorporated5 products
- Kenvue Brands LLC3 products
- Strategic Sourcing Services LLC1 product
- Wenzhou Yuyuan Pharmaceutical Co., Ltd.1 product
Recalls
From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific products or lots: check the name and lot number on your package.
-
September 11, 2026 · Class II · Ongoing · D-0006-2027
Lack of Assurance of Sterility
Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ (15 mL); a) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.com, NDC 70000-0502-1; b) Crocodile Tears, Distributed by: Crocodile Tears, Palm — K.C. Pharmaceuticals, Inc.
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.