Ehukai Beige Foundation Sunscreen Face Stick Broad Spectrum Spf 38
Product Images NDC 71014-023

2 FDA label images from Eai-jr 286, Inc · 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 Ehukai Beige Foundation Sunscreen Face Stick Broad Spectrum Spf 38 (NDC 71014-023). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eai-jr 286, Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Jjf Spf 38 Stick Update (2020 Jjf Spf 38 Art 4 Stick)

Jjf Spf 38 Stick Update (2020 Jjf Spf 38 Art 4 Stick)
Ehukai Beige Foundation Sunscreen Face Stick Broad Spectrum SPF 38 featuring a black cylindrical stick container with orange and white text. The label highlights the brand name Vertra and the SPF 38 protection. The active ingredient listed is Titanium Dioxide 23%. Labeler is Eai-jr 286, Inc, with manufacturing origin in Japan.*
FDA Label Image

Jjf Ekhui Beige Box Update (2020 Jjf Spf 38 Art 4)

Jjf Ekhui Beige Box Update (2020 Jjf Spf 38 Art 4)
The packaging label for Ehukai Beige Foundation Sunscreen Face Stick Broad Spectrum SPF 38 by Eai-jr 286, Inc. The label features the Vertra Premium Suncare logo and detailed Drug Facts, including active ingredient Titanium Dioxide 23%. It notes water resistance for 80 minutes, mineral-based formula, and Reef Safe certification. The package includes application directions, safety warnings, and ingredient lists. The product is a 11g (0.39 oz) stick in Ehukai Beige shade, with barcode and lot/expiration placeholders.*

* 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.