Quick answers
- What is Glycerin and povidone used for?
- The Drug Facts label of Ripple (CorneaCare Inc) lists these uses: For temporary relief of burning and irritation due to dryness of the eye; 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 irritation or to relieve dryness of the eye.
- Do I need a prescription for Glycerin and povidone?
- 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 Glycerin and povidone 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.
Ripple · CorneaCare Inc
Glycerin 0.63% · Povidone 0.25%, solution/ drops (ophthalmic)
Active ingredient
Glycerin 0.63% Povidone 0.25%
Purpose
Eye Lubricant
Uses
- For temporary relief of burning and irritation due to dryness of the eye.
- 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 irritation or to relieve dryness of the eye.
Warnings
For external use only
Do not use
- If solution changes color or becomes cloudy.
- lf you are sensitive to any ingredient in this product.
When using this product
- Do not touch tip of container to any surface to avoid contamination.
- Replace cap after using.
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 reach of children
If swallowed get medical help or contact a Poison Control Center (1-800-222-1222)right away. ►
Directions
Instill 1 or 2 drops in the eye(s) as needed.
Inactive ingredients
boric acid, calcium chloride, magnesium chloride, potassium chloride ,purified water, sodium borate, sodium chloride, sodium hyaluronate.
— FDA label of Ripple, CorneaCare Inc, effective May 24, 2026. See the official label on DailyMed →
Lacrifresh Hydramaxpf · Avizor, S.A.
Glycerin 0.25% · Povidone 0.4%, solution/ drops (ophthalmic)
Active ingredient
Purposes Glycerin 0.25% Lubricant Povidone 0.40% Lubricant
Purpose
For the temporary relief of burning and irritation due to dryness of the eye 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 or to relief dryness of the eye For use as a lubricant to prevent further irritation or to relief dryness of the eye
Uses
For the temporary relief of burning and irritation due to dryness of the eye 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 or to relief dryness of the eye For use as a lubricant to prevent further irritation or to relief dryness of the eye
Warnings
For external use only
Do not use
If solution changes color or becomes cloudy If you are sensitive to any ingredient in this product
When using this product
Do not touch tip of container to any surface to avoid contamination Replace cap after using
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 reach of children
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
Directions Instill 1 or 2 drops in the affected eye(s) as needed
Other information
Other information Store at 15º-30ºC (59º-86ºF) Discard the product within 90 days of first opening
Inactive ingredients
boric acid, calcium chloride, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium hyaluronate
Questions?
Questions or comments? Call: 1-800-714-1824
— FDA label of Lacrifresh Hydramaxpf, Avizor, S.A., effective October 27, 2025. 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.
Glycerin 0.63% · Povidone 0.25% · solution/ drops (ophthalmic) · 4 products
Glycerin 0.25% · Povidone 0.4% · solution/ drops (ophthalmic) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Lacrifresh Hydramaxpf | Avizor, S.A. | 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.
- Avizor, S.A.2 products
- CorneaCare Inc1 product
- Physician Recommended Neutraceuticals, L.P.1 product
- FSA Store Inc1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youA pharmacist can answer questions about this label
- Latest FDA drug recallsPrescription and over-the-counter, newest first
- All over-the-counter medicinesSearch by ingredient, brand or Spanish name
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.