Tinted Sunscreen
Product Images NDC 62932-213

9 FDA label images from Private Label Select Ltd Co · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Tinted Sunscreen (NDC 62932-213). 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

Active (Active Ingrediants)

Active (Active Ingrediants)
A Drug Facts panel listing the active ingredient Zinc Oxide at 22% concentration, used as a sunscreen agent.*
FDA Label Image

Dosage (Dosage And Administration)

Dosage (Dosage And Administration)
This image shows a directions panel for Tinted Sunscreen, providing instructions for application and sun protection measures. It advises applying generously 15 minutes before sun exposure, cautions for children under 6 months, and recommends limiting sun exposure during peak hours, wearing protective clothing, and reapplying after swimming, sweating, towel drying, or every two hours.*
FDA Label Image

Inactive Ingredient (Inactive Ingrediants)

Inactive Ingredient (Inactive Ingrediants)
Inactive ingredients list panel for Tinted Sunscreen by Private Label Select Ltd CO. The panel enumerates inactive ingredients including organic components such as Coconut Oil, Sunflower Seed Oil, Beeswax, Carnauba Wax, Shea Butter, Cocoa Seed Butter, Aloe Vera Leaf Juice, and Calendula Flower Extract, along with Titanium Dioxide and Iron Oxides.*
FDA Label Image

Indications (Indications And Usage)

Indications (Indications And Usage)
Text panel displaying Uses, Warnings, and Directions for Tinted Sunscreen by Private Label Select Ltd CO. It details sunburn prevention, cautions for external use only, avoidance on damaged skin, eye safety, keeping out of reach of children, and instructions to apply generously 15 minutes before sun exposure. It also includes sun protection measures and recommendations for limiting sun exposure.*
FDA Label Image

Keep Out Of Reach (Keep Out Of Reach)

Keep Out Of Reach (Keep Out Of Reach)
A safety warning panel advising to keep the product out of reach of children and to get medical help or contact Poison Control Center if the product is swallowed.*
FDA Label Image

Label (Label)

Label (Label)
Label for Earth Mama Lady Face Mineral Sunscreen, a tinted face stick with Broad Spectrum SPF 40. The product is moisturizing with mineral sun protection. It contains organic shea butter and cocoa butter, is water resistant for 40 minutes, and includes 22% zinc oxide as the active ingredient. The product is free from parabens, artificial fragrance, and is non-nano. Distributed by Earth Mama Angel Baby LLC, it is certified to NSF/ANSI 305 by Oregon Tilth and made in the USA.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
Drug Facts panel showing the active ingredient Zinc Oxide 22% listed with the purpose as Sunscreen.*
FDA Label Image

Unit Carton (Unit Carton)

Unit Carton (Unit Carton)
The packaging label for Earth Mama Lady Face Mineral Sunscreen Tinted Face Stick, SPF 40, Light/Medium Tint. The product is a moisturizing broad-spectrum tinted face stick with a net weight of 28 g (1.0 oz). The label includes drug facts, active ingredient (Sunscreen 10.15%), usage directions, a list of inactive ingredients, and emphasizes that it is reef-friendly, non-nano, and dermatologist tested. The labeler is Private Label Select Ltd CO, and the product is made in the USA.*
FDA Label Image

Warnings (Warnings)

Warnings (Warnings)
Warnings panel from the Tinted Sunscreen product label. It provides safety information including instructions for external use only, not to use on damaged or broken skin, warnings to keep out of eyes with rinsing instructions, advice to stop use and consult a doctor if rash occurs, and to keep the product out of reach of children with emergency instructions 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.