Sunmark Lubricant Eye Drops
Sunmark Lubricant Eye Drops is an FDA drug label for the active ingredient POLYPROPYLENE GLYCOL 400, PROPYLENE GLYCOL manufactured by Strategic Sourcing Services LLC administered by OPHTHALMIC. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231223.
- Generic name
- POLYPROPYLENE GLYCOL 400, PROPYLENE GLYCOL
- Manufacturer
- Strategic Sourcing Services LLC
- Product type
- HUMAN OTC DRUG
- Route
- OPHTHALMIC
- Dosage form
- N/A
- NDC
- 49348-947
- Application
- M018
- Label effective
- 20231223
About this product
Sunmark Lubricant Eye Drops is an FDA-registered drug product whose active ingredient is POLYPROPYLENE GLYCOL 400, PROPYLENE GLYCOL. It is labelled by Strategic Sourcing Services LLC taken by ophthalmic and marketed as a human otc drug product. Identifiers on file: NDC 49348-947, application M018, label effective 20231223. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing POLYPROPYLENE GLYCOL 400, PROPYLENE GLYCOL are most often described in connection with: temporary relief, irritation due. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses for the temporary relief of burning and irritation due to dryness of the eye
Dosage & Administration
Directions instill 1 or 2 drops in the affected eye(s) as needed children under 6 years of age: ask a doctor
Warnings
Warnings For external use only Do not use if this product changes color or becomes cloudy if you are sensitive to any ingredient in this product When using this product do not touch the tip of the 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(s) gets worse 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
Frequently asked questions
What is Sunmark Lubricant Eye Drops used for?
Uses for the temporary relief of burning and irritation due to dryness of the eye
Who makes Sunmark Lubricant Eye Drops?
Strategic Sourcing Services LLC is the labeler of record for Sunmark Lubricant Eye Drops.
What form does Sunmark Lubricant Eye Drops come in?
administered by ophthalmic. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Sunmark Lubricant Eye Drops prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Sunmark Lubricant Eye Drops been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.