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Over-the-counter medicine · no prescription needed

Carboxymethylcellulose, glycerin and polysorbate 80

Purpose on the label: Eye lubricant Eye lubricant Eye lubricant

Eye care

Official FDA data, not advice

The label text is quoted exactly as the company filed it with the U.S. Food and Drug Administration (FDA), with a link to the official copy. The list of brands comes from the FDA NDC Directory.

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.

If someone may have taken too much, call Poison Help: 1‑800‑222‑1222. In an emergency, call 911.

Quick answers

What is Carboxymethylcellulose, glycerin and polysorbate 80 used for?
The Drug Facts label of Refresh Optive Mega-3 PF (Allergan, Inc.) lists these uses: For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun. May be used as a protectant against further irritation.
Do I need a prescription for Carboxymethylcellulose, glycerin and polysorbate 80?
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 ingredients, 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 Carboxymethylcellulose, glycerin and polysorbate 80 been recalled?
No recall linked to these products appears in the FDA enforcement reports we use.

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.

Refresh Optive Mega-3 PF · Allergan, Inc.

Carboxymethylcellulose sodium 5 mg/mL · Glycerin 10 mg/mL · Polysorbate 80 5 mg/mL, solution/ drops (ophthalmic)

Active ingredient

Carboxymethylcellulose sodium 0.5% Glycerin 1% Polysorbate 80 0.5%

Purpose

Eye lubricant Eye lubricant Eye lubricant

Uses

For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun. May be used as a protectant against further irritation.

Warnings

For external use only. To avoid contamination, do not touch tip of container to any surface. Replace cap after using. If solution changes color, do not use.

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.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Prior to first use, please read the “Instructions for Use” inside this carton. Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

Use only if tape seals on top and bottom flaps are intact. Use before expiration date marked on container. Discard 90 days after opening. Store at 59°-77°F (15°-25°C). RETAIN THIS CARTON AND THE INSERT FOR FUTURE REFERENCE

Inactive ingredients

Boric acid; butylated hydroxyl toluene; carbomer copolymer type A; castor oil; erythritol; flaxseed oil; levocarnitine; polyoxyl 40 stearate; purified water; and trehalose. May contain hydrochloric acid and/or sodium hydroxide (to adjust pH).

Questions?

1.800.678.160 5 r efresheyedrops.com V1.0DFL3988

— FDA label of Refresh Optive Mega-3 PF, Allergan, Inc., effective March 1, 2026. See the official label on DailyMed →

Droptics Dry Eye Relief · Droptics LLC

Carboxymethylcellulose sodium 0.5% · Glycerin 1% · Polysorbate 80 0.5%, liquid (ophthalmic)

Active ingredient

Carboxymethylcellulose sodium 0.5% Glycerin 1% Polysorbate 80 0.5%

Purpose

Lubricant

Uses

For the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun For use as a protectant against further irritation

Warnings

For external use only

Do not use

if solution changes color

When using this product

  • Do not touch tip of the container to any surface to avoid contamination
  • Replace cap after each use

Stop use and ask a doctor if

  • If you feel eye pain
  • Changes in vision occur
  • Redness or irritation of the eye lasts
  • Condition worsens or lasts more than 72 hours

Keep out of reach of children

  • If swallowed, get medical help or contact a Poison Control Center right away

Directions

Put 1 or 2 drops in the affected eye(s) as needed. Tightly screw on cap to seal after use.

Inactive ingredients

L-arginine (amino acid), boric acid, cyanocobalamin (Vitamin B12), edetate disodium, potassium chloride, purified water, pyridoxine hydrochloride (Vitamin B6), sodium chloride, sodium citrate, stabilized oxychloro complex, taurine (amino acid), tocopherol acetate (Vitamin E), trehalose, sodium hydroxide and/or hydrochloric acid (to adjust pH)

— FDA label of Droptics Dry Eye Relief, Droptics LLC, effective July 22, 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 ingredients, 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.

Carboxymethylcellulose sodium 5 mg/mL · Glycerin 10 mg/mL · Polysorbate 80 5 mg/mL · solution/ drops (ophthalmic) · 8 products

Drug Facts for this strength and form ↑

Carboxymethylcellulose sodium 0.5% · Glycerin 1% · Polysorbate 80 0.5% · liquid (ophthalmic) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Droptics Dry Eye Relief Droptics LLC DailyMed

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Carboxymethylcellulose, glycerin and polysorbate 80, by strength and form
Strength and formGeneric or brandPharmacies pay
carboxymethylcellulose sodium 5 mg/mL · glycerin 10 mg/mL · polysorbate 80 5 mg/mL
solution/ drops
Brand: REFRESH OPTIVE Advanced $0.4458 per unit
carboxymethylcellulose sodium 5 mg/mL · glycerin 10 mg/mL · polysorbate 80 5 mg/mL
solution/ drops
Brand: REFRESH OPTIVE Advanced $1.03 per mL
carboxymethylcellulose sodium 5 mg/mL · glycerin 10 mg/mL · polysorbate 80 5 mg/mL
solution/ drops
Brand: REFRESH Optive Mega-3 $0.4458 per unit
carboxymethylcellulose sodium 5 mg/mL · glycerin 10 mg/mL · polysorbate 80 5 mg/mL
solution/ drops
Brand: Refresh Digital $1.03 per mL
carboxymethylcellulose sodium 5 mg/mL · glycerin 10 mg/mL · polysorbate 80 5 mg/mL
solution/ drops
Brand: Refresh Digital PF $0.4458 per unit

NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

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.

Recalls

No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.

Next steps

Sources

  1. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  4. 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.

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