Aluroderm Scar Patch
Product Images NDC 84991-0316

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Aluroderm Scar (NDC 84991-0316). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Olakino Therapeutics Llc, 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

Box (Aluroderm Box 12.4.24 Final)

Packaging label for Aluroderm Scar Patch containing 0.75% allantoin. The label shows the product name in prominent teal and purple font, specifying it is a scar patch with 5 patches per package. The labeler is Olakino Therapeutics LLC, with a visible barcode and product NDC 84991-0316-1. Additional text on the label includes inactive ingredients and usage warnings, with a decorative circle pattern in shades of teal and purple.*

FDA Label Image

Pouch (Aluroderm Pouch Listing Image)

Aluroderm Scar Patch carton packaging displaying the proprietary name Aluroderm and the active ingredient allantoin at 0.75% strength. The label indicates that the product contains 5 patches and includes additional ingredients hyaluronic acid and taxifolin. The labeler is Olakino Therapeutics LLC with NDC 84991-0316-5. The front and back of the packaging are shown, featuring the product name, strength, dosage form (patch), and manufacturer details.*

* 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.