Active Ingredient
Carboxymethylcellulose sodium 1%
Dry Eye Relief Gel
FDA Label NDC 70000-0089
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health 110, Llc. Dba Leader for the product Dry Eye Relief (NDC 70000-0089). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Eye lubricant
Uses
- For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun.
- for used as a protectant against further irritation or to relieve dryness of the eye.
Warnings
- For external use only.
- To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
- If solution changes color or becomes cloudy, do not use.
Directions
Instill 1 or 2 drops in the affected eye(s) as needed.
Other Information
- Use only if imprinted tape seals on top and bottom flaps are intact and clearly legible.
- Use before expiration date marked on container.
- Discard 90 days after opening.
- Store at 59°-86°F (15°-30°C).
- RETAIN THIS CARTON FOR FUTURE REFERENCE.
Inactive Ingredients
Boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; stabilized oxychloro complex; sodium borate; and sodium chloride, May Contain Hydrochloric Acid and /or Sodium hydroxide to adjust PH.
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