Lbel Nude Skin Ultra Light Matte Foundation With Vitamins Spf 20 Capuccino 310-c Emulsion
Product Images NDC 14141-019

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Lbel Nude Skin Ultra Light Matte Foundation With Vitamins Spf 20 Capuccino 310-c (NDC 14141-019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bel Star S.a., 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

230-n (Almendra 230 N Page 0001)

230-n (Almendra 230 N Page 0001)
Label packaging for LBEL Nude Skin Ultra Light Matte Foundation with Vitamins SPF 20 beige 220-C, an emulsion topical sunscreen with active ingredients octinoxate 6.00% and zinc oxide 2.94%. The label includes drug facts and directions, SPF 20 protection, descriptor "ultra-light matte foundation with vitamins," and a depiction of the product bottle. The product volume is 0.87 fl.oz. (26 ml) and the labeler is Bel Star S.A.*
FDA Label Image

220-c (Beige 220 C Page 0001)

220-c (Beige 220 C Page 0001)
Packaging label for LBEL NUDE SKIN ULTRA LIGHT MATTE FOUNDATION WITH VITAMINS SPF 20 BEIGE 220-C. The label shows it as an ultra-light matte foundation with SPF 20, in beige tone 220-C, with active ingredients Octinoxate 6.00% and Zinc Oxide 2.94%, both sunscreens. The label includes drug facts, warnings, directions, full ingredient list, and the labeler Bel Star S.A. The product is a topical emulsion in a 0.87 fl oz (26 ml) container.*
FDA Label Image

310-c (Capuccino 310 C Page 0001)

310-c (Capuccino 310 C Page 0001)
Packaging label for LBEL Nude Skin Ultra Light Matte Foundation with Vitamins SPF 20 Beige 220-C. The label shows product name, SPF 20, dosage form as emulsion, volume 0.87 fl oz (26 ml), and the labeler Bel Star S.A. It includes drug facts with active ingredients Octinoxate 6.00% and Zinc Oxide 2.94% as sunscreens, warnings, uses, directions, inactive ingredients, and a graphic of the foundation bottle with a dropper. The tone is labeled as Capuccino 310-C.*
FDA Label Image

170-n (Champagne 170 N Page 0001 (2))

170-n (Champagne 170 N Page 0001 (2))
Packaging label for L'BEL Nude Skin Ultra Light Matte Foundation with Vitamins SPF 20, shade Champagne 170-N. The topical emulsion contains octinoxate 6.00% and zinc oxide 2.94% as active sunscreen ingredients. The package includes Drug Facts with active/inactive ingredients, directions, warnings, and other product details. The labeler is Bel Star S.A. and the net volume is 0.87 fl oz (26 ml).*
FDA Label Image

180-f (Latte 180 F Page 0001)

180-f (Latte 180 F Page 0001)
Packaging label for L'BEL NUDE SKIN Ultra Light Matte Foundation with Vitamins SPF 20 in shade Beige 220-C. The emulsion is topical and comes in a 0.87 fl. oz. (26 ml) size. Active ingredients include octinoxate 6.00% and zinc oxide 2.94% as sunscreens. Labeler is Bel Star S.A. The label also includes directions, warnings, ingredients, usage information, and a small illustration of the dropper bottle product container.*
FDA Label Image

390-n (Mokaccino 390 N Page 0001)

390-n (Mokaccino 390 N Page 0001)
Packaging label for LBEL Nude Skin Ultra Light Matte Foundation with Vitamins SPF 20 Beige 220-C, a topical emulsion sunscreen with active ingredients octinoxate 6.00% and zinc oxide 2.94%. The label includes drug facts with warnings, uses, directions, and a list of inactive ingredients. The product is in a 0.87 fl. oz. (26 ml) container and labeled by Bel Star S.A. The label features the brand name L'BEL, product name, and an illustration of a dropper bottle.*

* 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.