Clearskin Blackhead Eliminating
Product Images NDC 10096-0320

3 FDA label images from New Avon Llc · 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 Clearskin Blackhead Eliminating (NDC 10096-0320). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by New Avon 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

Image Of Back Label (Dfb1)

Image Of Back Label (Dfb1)
Drug Facts panel of Clearskin Blackhead Eliminating Daily Astringent showing active ingredient Salicylic Acid 2.0% for acne treatment. The panel lists uses including treatment of acne, clearing up blackheads, and prevention of new blackheads.*
FDA Label Image

Image Of Back Label (Dfb2)

Image Of Back Label (Dfb2)
This image shows the 'Warnings' and 'Directions' sections of the Drug Facts label for Clearskin Blackhead Eliminating Daily Astringent by New Avon LLC. It includes instructions for safe use, precautions regarding eye contact, skin irritation, and flammability, directions for application frequency and technique, and a note on reducing usage if dryness occurs. The label also lists inactive ingredients and provides contact numbers for questions in the US and Canada.*
FDA Label Image

Image Of Pdp (Pdp)

Image Of Pdp (Pdp)
The label for Clearskin Blackhead Eliminating Daily Astringent by New Avon LLC shows the product name prominently along with the active ingredient, Salicylic Acid 2.0%. The label also indicates the product is a liquid acne treatment and provides multilingual descriptions. The volume is 250 ml (8.4 fl oz).*

* 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.