Hydrating Glow Mist With Pentavitin Spray
Product Images NDC 81104-017

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydrating Glow Mist With Pentavitin (NDC 81104-017). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Naked Sundays Pty Ltd, 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

30 mL (Naked Sundays 30 mL Label)

Label for Hydrating Glow Mist with Pentavitin SPF 50 Broad Spectrum sunscreen top up spray. The product is a 30 mL (1.01 fl. oz.) topical spray. The label displays the active ingredients Avobenzone 3%, Homosalate 10%, Octisalate 5%, and Octocrylene 5%, each serving as a sunscreen. The label includes a Drug Facts panel with warnings, usage instructions, and other regulatory details. Labeler is Naked Sundays Pty Ltd.*

FDA Label Image

Fold Out (Naked Sundays 30 mL Label 2)

Drug Facts panel continuing warnings, directions, sun protection measures, inactive ingredients such as citric acid, watermelon seed oil, and others, plus other information about product protection and contact information for Naked Sundays Pty Ltd. The panel includes safety precautions like flammability warnings and usage instructions for Hydrating Glow Mist with SPF 50.*

FDA Label Image

75 mL (Naked Sundays 75 mL Label)

Label for Hydrating Glow Mist with Pentavitin SPF 50 Broad Spectrum sunscreen spray, topical use, from Naked Sundays Pty Ltd. The label lists active ingredients Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 6%. It specifies broad spectrum SPF 50 protection in a 75 mL (2.53 fl oz) spray bottle. The label also includes directions, warnings, inactive ingredients, and manufacturer information.*

* 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.