Powder
Product Images NDC 61354-119

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 Powder (NDC 61354-119). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Oxygen Development 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

61354-119-02_aw (00 4 In 1 Pressed Mineral Fc Nov2022 Final All Page 09)

61354-119-02_aw (00 4 In 1 Pressed Mineral Fc Nov2022 Final All Page 09)
Packaging label for Powder topical powder with Titanium Dioxide as the active ingredient. The label shows the brand PUR and describes the product as a 4-in-1 pressed mineral makeup with broad-spectrum SPF 15. The label includes bilingual text in English and French, a barcode, and color references for print. The manufacturer is Pur Cosmetics with product details and warnings outlined.*
FDA Label Image

61354-119-01-aw (09 4 In 1 Pressed 0.28oz Bl Blush Medium Mp3 Mar2022 Us Ol)

61354-119-01-aw (09 4 In 1 Pressed 0.28oz Bl Blush Medium Mp3 Mar2022 Us Ol)
A packaging label layout from Standwill Packaging, Inc. showing multiple shaped panels with printed text for a topical powder product. The design includes dimensions and specifications for glue areas, no ink zones, and five text panels presenting ingredient and usage information. The label uses 100% black ink on white clear backing, indicated for a 0.75 inch diameter size. No specific product branding or strengths visible related directly to Titanium Dioxide or the Powder product by Oxygen Development LLC.*
FDA Label Image

61354-119-01_aw (Compact Astral)

* 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.