Neutrogena Skinclearing Mineral Powder Natural Ivory 20 Powder
Product Images NDC 69968-0839

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Neutrogena Skinclearing Mineral Powder Natural Ivory 20 (NDC 69968-0839). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kenvue Brands 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

0833 (0833)

0833 (0833)
Neutrogena SkinClearing Mineral Powder Chestnut 135 in powder form. The round pink label indicates it contains Salicylic Acid 0.5% as the active ingredient for acne treatment. The net weight is 0.38 oz (11 g). Distributed by Johnson & Johnson Consumer Inc. The label includes Drug Facts and application tips for use as a blemish treatment and mattifying powder.*
FDA Label Image

0834 (0834)

0834 (0834)
Label for Neutrogena SkinClearing Mineral Powder Honey 85 topical powder containing 0.5% salicylic acid. The label includes product details such as the brand name, active ingredient, net weight of 0.38 oz (11 g), and distribution by Johnson & Johnson Consumer Inc. It highlights the 2-in-1 function to cover, treat, and help prevent breakouts with MicroClear technology. The label also features Drug Facts with usage instructions, warnings, inactive ingredients, and contact information.*
FDA Label Image

0835 (0835)

0835 (0835)
Neutrogena SkinClearing Mineral Powder Natural Beige 60, topical powder for acne treatment with 0.5% salicylic acid. The label includes drug facts, active ingredient, purpose, warnings, directions, and inactive ingredients. The product is distributed by Johnson & Johnson Consumer Inc.*
FDA Label Image

0836 (0836)

0836 (0836)
Neutrogena SkinClearing mineral powder Soft Beige 50 label featuring Salicylic Acid 0.5% as the active ingredient in powder form. The label highlights its use for acne treatment and includes Drug Facts, warnings, directions, and a net weight of 0.38 oz (11 g). Distributed by Johnson & Johnson Consumer Inc.*
FDA Label Image

0837 (0837)

0837 (0837)
Neutrogena SkinClearing Mineral Powder Nude 40 is a topical powder with 0.5% salicylic acid active ingredient. The label, pink in color, features application tips and drug facts including warnings, directions, inactive ingredients, and contact information. The net weight is 0.38 oz (11 g), and the labeler is Johnson & Johnson Consumer Inc.*
FDA Label Image

0838 (0838)

0838 (0838)
Neutrogena SkinClearing Mineral Powder Buff 30, a topical powder containing 0.5% salicylic acid, distributed by Johnson & Johnson Consumer Inc. The label highlights its use as a blemish treatment with MicroClear technology, oil-absorbing powder, and application tips. The net weight is 0.38 oz (11 g), with Drug Facts and warnings included.*
FDA Label Image

0839 (0839)

0839 (0839)
Drug Facts panels for Neutrogena SkinClearing mineral powder Natural Ivory 20 show active ingredient Salicylic Acid (0.5%) for acne treatment. The panels list warnings, directions, inactive ingredients including Mica, Dimethicone, and others, and usage instructions. Contact information and storage advice are also included.*
FDA Label Image

0840 (0840)

0840 (0840)
Packaging label for Neutrogena SkinClearing mineral powder Classic Ivory 10, an OTC topical powder containing 0.5% salicylic acid for acne treatment. The label highlights features such as MicroClear technology and oil absorbing powder, and provides net weight of 0.38 oz (11 g). It is labeled by Johnson & Johnson Consumer Inc., with directions and warnings included in a peel-back Drug Facts section.*

* 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.