Rugby Lubricating Drops
Rugby Lubricating Drops is an FDA drug label for the active ingredient POLYVINYL ALCOHOL manufactured by A-S Medication Solutions 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 20231110.
- Generic name
- POLYVINYL ALCOHOL
- Manufacturer
- A-S Medication Solutions
- Product type
- HUMAN OTC DRUG
- Route
- OPHTHALMIC
- Dosage form
- N/A
- NDC
- 50090-5996
- Application
- M018
- Label effective
- 20231110
About this product
Rugby Lubricating Drops is an FDA-registered drug product whose active ingredient is POLYVINYL ALCOHOL. It is labelled by A-S Medication Solutions taken by ophthalmic and marketed as a human otc drug product. Identifiers on file: NDC 50090-5996, application M018, label effective 20231110. It is one of 2 FDA drug label records sharing the active ingredient POLYVINYL ALCOHOL. 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 POLYVINYL ALCOHOL are most often described in connection with: temporary relief, discomfort due, minor irritations, eye exposure, wind sun, protectant against. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses for 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
Dosage & Administration
Directions instill 1 to 2 drops in the affected eye(s) as needed
Warnings
Warnings Do not use if solution changes color or becomes cloudy When using this product do not touch tip of container to any surface to avoid contamination remove contact lens before using. replace cap after using. keep container tightly closed 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
More products with the same ingredient
POLYVINYL ALCOHOLHow products containing POLYVINYL ALCOHOL compare
FDA lists 2 drug label records with POLYVINYL ALCOHOL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | A-S Medication Solutions | 1 |
| — | — | AvPAK | 1 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Recall and safety notices
5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0292-2025 | METFORMIN HYDROCHLORIDE EXTENDED- RELEASE 500MG, 180 TABLETS, Packaged BY: A-S Medication Solutions, Libertyville, IL 60048 NDC 50090-1494-3. | A-S Medication Solutions LLC | Class II | Ongoing | 20250402 |
| D-0631-2024 | Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2 | A-S Medication Solutions LLC | Class I | Terminated | 20240814 |
| D-0096-2022 | Cetirizine hydrochloride, 10 mg tablets, 90-count bottle, Distributed by: A-S Medications Solutions, Libertyville, IL 60048, Mfg: Major Pharmaceuticals, Livonia, MI 48152, NDC: 50090-5510-3 | A-S Medication Solutions LLC. | Class III | Terminated | 20211117 |
| D-0358-2021 | Acetaminophen, Extra Strength, Aspirin Free, 500 MG Tablets, 100-count bottles, Mfr: Major Pharmaceuticals, Livonia, MI 48152; Packaged Exclusively By: A-S Medication Solutions LLC, Libertyville, IL 60048, Product # 6967-0; NDC: 50090-5350-0; contained within Health Essentials Kit, Kit Contains: 1 bottle hand sanitzer, 1 reusable face mask, 1 bottle Acetaminophen 500 mg, 1 bag cough drops, 1 digital thermometer, 50 disposable gloves. | A-S Medication Solutions LLC. | Class I | Terminated | 20210512 |
| D-1110-2018 | Valsartan and Hydrochlorothiazide Tablets, Valsartan 160 MG and Hydrochlorothiazide 12.5 MG, 90 tablets per bottle, Rx Only, MFG: Arrow Pharm (Malta) LTD, Birzebbugia, BBG 3000 Malta. NDC: 54569-6480-0 | A-S Medication Solutions LLC. | Class II | Ongoing | 20180829 |
Frequently asked questions
What is Rugby Lubricating Drops used for?
Uses for 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
Who makes Rugby Lubricating Drops?
A-S Medication Solutions is the labeler of record for Rugby Lubricating Drops. 2 FDA label records share the active ingredient POLYVINYL ALCOHOL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does Rugby Lubricating 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 Rugby Lubricating 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.
Are there other products containing POLYVINYL ALCOHOL?
Yes. 2 FDA drug label records list POLYVINYL ALCOHOL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has Rugby Lubricating Drops been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
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.