Rugby Lubricating Drops Solution/ Drops
FDA Label NDC 50090-5996

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by A-s Medication Solutions for the product Rugby Lubricating Drops (NDC 50090-5996). 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, when using this product, keep out of reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Polyvinyl Alcohol 1.4%

Purpose

Lubricant

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

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

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • instill 1 to 2 drops in the affected eye(s) as needed

Other Information

  • store at room temperature
  • keep tightly closed
  • replace cap after use
  • retain carton for full drug facts

Inactive Ingredients

dibasic sodium phosphate, edetate disodium, monobasic sodium phosphate,

purified water, sodium chloride. Phosphoric acid and/or sodium hydroxide may be added to adjust pH. PRESERVATIVE ADDED: benzalkonium chloride 0.01%

Questions ?

Call 1-800-645-2158

How Supplied

Product: 50090-5996

NDC: 50090-5996-0 15 mL in a BOTTLE

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