Rite Aid Decolorized Iodine Liquid
Product Images NDC 11822-6450

3 FDA label images from Rite Aid Corporation · 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 Rite Aid Decolorized Iodine (NDC 11822-6450). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rite Aid Corporation, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Label (Doc110717 (003))

Label (Doc110717 (003))
The packaging label for Rite Aid Decolorized Iodine contains denatured alcohol 48% as the active ingredient. It is a 2 FL OZ (59 mL) topical antiseptic solution in liquid form. The label prominently displays warnings about flammability, advising to keep away from spark, heat, or flame. The labeler is Rite Aid Corporation, with distribution at 30 Hunter Lane, Camp Hill, PA 17011. The barcode and item number 0306450 are shown on the label.*
FDA Label Image

Ra Decolorized 032021.jpg

Ra Decolorized 032021.jpg
Label for Rite Aid Decolorized Iodine with 48% Ethyl Alcohol topical liquid, 2 FL OZ (59 mL). The label highlights the product as a first aid antiseptic and includes Drug Facts with active ingredient, indications, warnings, directions, and storage information. Distributed by Rite Aid Corporation.*
FDA Label Image

Radecorized

Radecorized
Rite Aid Decolorized Iodine iodides tincture antiseptic liquid, 2 fl oz (59 mL) bottle label. Contains ethyl alcohol 0.45 mL/mL as the active ingredient. The label includes warnings about flammability and usage instructions. Distributed by Rite Aid Corporation, Camden Hill, PA.*

* 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.