Plus Rinse Emergency Eyewash Liquid
Product Images NDC 72598-022

3 FDA label images from Innovative Safety Supply Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Plus Rinse Emergency Eyewash (NDC 72598-022). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Innovative Safety Supply Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Pic1

Pic1
Drug Facts panel from Plus Rinse Emergency Eyewash with purified water 99.1% as the active ingredient. It includes usage instructions for rinsing eyes to reduce injury risk, warnings for external use only, directions for use, other information about storage and expiration, and a contact number for questions. The label also shows manufacturer and distributor details and refill code information.*
FDA Label Image

Pic2

Pic2
Label for Plus Rinse Emergency Eyewash 1000 mL sterile ophthalmic liquid. The label shows the product name, NDC 72598-022-01, compliance to ANSI/ISEA Z358.1-2014, and the labeler Innovative Safety Supply Inc. The label includes usage instructions illustrations and the company logo.*
FDA Label Image

Pic3

Pic3
Plus Rinse Emergency Eyewash label showing the proprietary name and NDC 72598-022-02. The label states compliance with ANSI/ISEA Z358.1-2014 standard for personal eyewash. It includes the labeler information: Innovative Safety Supply Inc., Saskatoon, Canada. The product is sterile liquid, 200 mL (6.8 fl oz) in volume. The label features branding and instructions for use pictogram.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.