Skin1004 Madagascar Centella Hyalu-cica Water-fit Sun Serum Uv Cream
Product Images NDC 85796-2805

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Skin1004 Madagascar Centella Hyalu-cica Water-fit Sun Serum Uv (NDC 85796-2805). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Craver Corporation, 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

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38da3f8a Dc92 D121 E063 6394a90a083e
Packaging label for SKIN1004 Madagascar Centella Hyalu-Cica Water-Fit Sun Serum UV Broad Spectrum SPF 50 sunscreen cream, 50 mL (1.69 fl. oz.), distributed by Craver Corporation. The front features water imagery and lists the product as made with pure Centella from Madagascar. The label includes drug facts with active ingredients: Butyl Methoxydibenzoylmethane 2.7%, Ethylhexyl Salicylate 4.5%, Homosalate 13.6%, and Octocrylene 9%, all sunscreens. The label also provides usage directions, warnings, and inactive ingredient details, indicating moisturizing care and topical route.*
FDA Label Image

Jpg (Artwork Otc Craver)

Jpg (Artwork Otc Craver)
Packaging label for SKIN1004 Madagascar Centella Hyalu-Cica Water-Fit Sun Serum UV broad spectrum SPF 50 sunscreen cream. The label features blue water imagery and includes drug facts stating active ingredients: Butyl Methoxydibenzoylmethane 2.7%, Ethylhexyl Salicylate 4.5%, Homosalate 13.6%, Octocrylene 9%. It indicates moisturizing care with Centella Asiatica extract from Madagascar and a 50 mL (1.69 FL. OZ.) container. Manufactured by Craver Corporation.*

* 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.