Refreshbrand.com (Refresh Relieva Preservative Free Unit Dose 01)
Refresh Relieva Pf Solution/ Drops
Product Images NDC 0023-4515
View Photos of 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 Refresh Relieva Pf (NDC 0023-4515). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Allergan, 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.
Refreshrelieva Pflubricates And Protectsalso Relieves Lasik Drynessnew!preservative-free30 Vials 0.01 Fl Oz (0.4 mL) Sterile (Refresh Relieva Preservative Free Unit Dose 02)
The image shows the unfolded packaging label for Refresh RELIEVA PF ophthalmic solution/drops by Allergan, Inc. The front panel highlights the product name 'Refresh RELIEVA PF' as a preservative-free lubricant recommended for sensitive eyes. The label includes active ingredients Carboxymethylcellulose sodium and Glycerin, dosage form as solution/drops, and a 30 vial count of 0.4 mL unit doses. Additional panels provide drug facts, directions, and warnings.*
Refresh Relieva Preservative Free Unit Dose 03
The image shows the carton packaging for Refresh RELIEVA PF ophthalmic solution/drops. The front panel displays the product name Refresh RELIEVA PF with a graphic of a drop. The carton states it is recommended for sensitive eyes and contains 5 vials, each 0.4 mL. The label includes active ingredients Carboxymethylcellulose sodium and Glycerin. The labeler is Allergan, Inc. Drug Facts panels with usage, warnings, directions, and inactive ingredients are visible on the sides and back of the carton.*
* 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.
