Active Ingredient
Purified Water 99.1%
Eye Wash Solution
FDA Label NDC 49687-0010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cmc Group Inc. for the product Eye Wash (NDC 49687-0010). 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, use, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Eyewash
Use
- For cleansing the eye to help relieve irritaion or burning by removing loose foreign material
Warnings
For external use only.
Do Not Use
if solution changes color or becomes cloudy
When Using This Product
- to avoid contamination, do not touch tip of container to any surface
- do not reuse
- once opened, discard
- obtain immediate medical treatment for all open wounds in or near the eyes
Stop Use And Ask A Doctor If
you experience:
- eye pain
- changes in vision
- continued redness
- irritation of the eye
- condition worsens or perisists
Keep Out Of Reach Of Children.
If swallowed, get medical help of contact a Poison Control Center right away.
Directions
- Flush the affected eyes as needed, controlling the rate of flow of solution by pressure on the bottle
Other Information
- not for use as contact len solution
- use before expiration date marked on the bottle
- store at room temperature, 5 o to 35 oC (41 o to 95 oF)
Inactive Ingredients
Benzalkonium chloride, sodium chloride
* Please review the disclaimer below.
