Eai-jr286, Inc Vertra Sensitive Spf 30 Sunscreen Face Stick
Product Images NDC 62932-263

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Eai-jr286, Inc Vertra Sensitive Spf 30 Sunscreen Face Stick (NDC 62932-263). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Private Label Select Ltd Co, 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

Otc Active Ingredients (Active Purpose)

Otc Active Ingredients (Active Purpose)
Drug Facts panel showing active ingredient Zinc Oxide 20% with its purpose listed as Sunscreen. The panel is part of the labeling for EAI-JR286, Inc Vertra Sensitive SPF 30 Sunscreen Face Stick by Private Label Select Ltd CO.*
FDA Label Image

Artwork (Back Inner)

Artwork (Back Inner)
Drug Facts panel from EAI-JR286, Inc Vertra Sensitive SPF 30 Sunscreen Face Stick. This text panel includes Active Ingredients listing zinc oxide 20%, Purpose as sunscreen, Warnings for external use only, directions for application 15 minutes before sun exposure, reapplication instructions, and notes about keeping out of children's reach, especially under 6 months of age. Labeler information indicates it is made in the USA by Private Label Select Ltd CO in Torrance, CA.*
FDA Label Image

Directions And Administration (Directions)

Directions And Administration (Directions)
Directions for use of EAI-JR286, Inc Vertra Sensitive SPF 30 Sunscreen Face Stick. Instructions include applying liberally 15 minutes before sun exposure and reapplying at least every 2 hours. Advises consulting a doctor for children under 6 months. Contains sun protection recommendations such as limiting sun time from 10 a.m. to 2 p.m., wearing protective clothing, and reapplying after swimming, sweating, or towel drying.*
FDA Label Image

Artwork (FRONT)

Artwork (FRONT)
Label of Vertra Sensitive SPF 30 Sunscreen Face Stick showing 10.5g (0.37 oz) net weight. The label indicates it is a broad-spectrum SPF 30 sunscreen face stick, water resistant for 80 minutes, with the brand name Vertra and the descriptor 'Sensitive' prominently displayed in orange and black text on a white background.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
A text panel listing the inactive ingredients of EAI-JR286, Inc Vertra Sensitive SPF 30 Sunscreen Face Stick. It includes various oils, waxes, butters, and plant extracts such as coconut oil, sunflower seed oil, beeswax, shea butter, castor seed oil, cocoa seed butter, and aloe vera leaf juice, with several ingredients marked as certified organic.*
FDA Label Image

Outer Packaging (Outer Packaging)

Outer Packaging (Outer Packaging)
This image shows the drug facts and product information for Vertra Premium Suncare Sensitive SPF 30 Mineral Based Sunscreen Face Stick. It lists active ingredient zinc oxide 20% as sunscreen, usage directions, warnings, and other information about sun protection, application, and ingredients. The product is water resistant for 80 minutes, fragrance-free, reef safe, and contains 70% certified organic ingredients. It is distributed by Vertra, EAI-JR286, Inc.*
FDA Label Image

Indications And Usage (Uses)

Indications And Usage (Uses)
Text panel titled "Uses" describing benefits of the product including helping prevent sunburn, reducing risk of skin cancer and early skin aging if used with other sun protection measures, higher SPF providing more sunburn protection, retaining SPF after 80 minutes of water exposure or sweating, and providing high protection against sunburn.*
FDA Label Image

Warnings (Warnings)

Warnings (Warnings)
Warning label from EAI-JR286, Inc Vertra Sensitive SPF 30 Sunscreen Face Stick by Private Label Select Ltd CO. It advises against use on damaged or broken skin, instructs to keep out of eyes and rinse with water if contact occurs, and to stop use and consult a doctor if rash or irritation develops. It specifies external use only and warns to keep out of reach of children, seeking medical help if swallowed.*

* 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.