Leader Lubricant Eye Drops
Leader Lubricant Eye Drops is an FDA drug label for the active ingredient CARBOXYMETHYLCELLULOSE SODIUM manufactured by Cardinal Health 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: CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer: Cardinal Health
Product Type: HUMAN OTC DRUG
Route: OPHTHALMIC
Dosage Form:
NDC: 70000-0012
Application: M018
Effective: 20231223
Active Ingredients: Active ingredients Carboxymethylcellulose sodium 0.5%
Indications & Usage
Uses for the temoprary 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 the reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1800-222-1222) immediately.
Adverse Reactions
Not available.
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