Rugby Lubricant Eye Drops

CARBOXYMETHYLCELLULOSE SODIUM OPHTHALMIC HUMAN OTC DRUG

Rugby Lubricant Eye Drops is an FDA drug label for the active ingredient CARBOXYMETHYLCELLULOSE SODIUM manufactured by Rugby Laboratories 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 20231220.

Generic name
CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer
Rugby Laboratories
Product type
HUMAN OTC DRUG
Route
OPHTHALMIC
Dosage form
N/A
NDC
0536-1387
Application
M018
Label effective
20231220

Active ingredients

Active ingredient Carboxymethylcellulose sodium 0.5%

Indications & Usage

Uses for temporary relief of burning, irritation, and discomfort due to dryness of the eyes or exposure to wind or sun may be used as a protectant against further irritation

Dosage & Administration

Directions to open, twist and pull tab to remove instill 1 or 2 drops in the affected eye(s) as needed and discard container if used for post-operative, (e.g., LASIK) dryness and discomfort, follow your eye doctor's instructions

Contraindications

Not available.

Warnings

Warnings For external use only Do not use this product if solution changes color or becomes cloudy When using this product do not reuse once opened, discard to avoid contamination, do not touch tip of container to any surface do not touch unit-dose tip to eye Stop use and ask a doctor if you experience eye pain changes in vision occur redness or irritation of the eye continues redness or irritation of the eye worsens or persists for more than 72 hours Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Adverse Reactions

Not available.

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