Quick answers
- What is Naphazoline and propylene glycol used for?
- The Drug Facts label of Droptics Performance Eye Drops (Droptics LLC) lists these uses: Temporarily relieves burning and irritation due to dryness of the eye Relieves redness of the eye due to minor eye irritations.
- Do I need a prescription for Naphazoline and propylene glycol?
- 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 Naphazoline and propylene glycol 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.
Droptics Performance Eye Drops · Droptics LLC
Naphazoline hydrochloride 0.03% · Propylene glycol 1%, liquid (ophthalmic)
Active ingredient
Naphozoline Hydrochloride 0.03% Propylene Glycol: 1.0%
Purpose
Redness Reliver Lubricant
Uses
Temporarily relieves burning and irritation due to dryness of the eye Relieves redness of the eye due to minor eye irritations
Warnings
For external use only
Ask a doctor before use if
you have narrow angle glaucoma
When using this product
- Do not touch tip of container to any surface to avoid contamination
- Replace each cap after each use
Do not use
if solution changes color or becomes cloudy
- Overuse may cause more eye redness
- Pupils may become enlarged temporarily
- Remove contact lenses before use Stop Use and ask a doctor if
- You feel eye pain
- Changes in vision occur
- Redness or irritation of the eyes 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) up to 4 times daily Tightly screw on cap to seal after use
Inactive ingredients
benzalkonium chloride, boric acid, borneol, caffeine, camphor, menthol, potassium l-aspartate, purified water, taurine
— FDA label of Droptics Performance Eye Drops, Droptics LLC, effective February 9, 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.
Naphazoline hydrochloride 0.03% · Propylene glycol 1% · liquid (ophthalmic) · 2 products
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.
- Revitalize Energy Inc.1 product
- Droptics LLC1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
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.