Eys Eye Wash Solution
FDA Label NDC 57349-220

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Eyes-plus Llc for the product Eys Eye Wash (NDC 57349-220). 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 other, active ingredient, purpose, use, warnings, otc - 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

Other

Drug Facts

Active Ingredient

Purified Water USP 98.4%

Purpose

Eyewash

Use

For cleansing the eye to help relieve irritation by removing loose foreign material

Warnings

  • To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard
  • If you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists, consult a doctor
  • Obtain immediate medical treatment for all open wounds in or near the eyes If solution changes color or becomes cloudy do not use

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Directions

Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle

Other Information

  • Store at 41° to 85°F
  • Do not use if top is broken or missing

Inactive Ingredients

boric acid, sodium borate, sodium chloride, sorbic acid

Principal Display Panel - 15 Ml Vial Label

OPEN

EyS
Eye Wash
0.5 fl. oz. (15 ml)

STERILE A

Principal Display Panel (15 ml Vial Label)

Principal Display Panel (15 ml Vial Label)

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