Organys Derma Made Lotion
Product Images NDC 83612-0330

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 Organys Derma Made (NDC 83612-0330). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Organys Beauty, 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

Pdp (Pdp)

Pdp (Pdp)
Drug Facts panel for Organys Derma Made Tinted Mineral Lotion SPF 50+ with 12% Zinc Oxide as the active ingredient. Includes uses, warnings, directions, inactive ingredients, and other information such as water resistance for 80 minutes and broad spectrum sun protection. The label mentions it is dermatologist developed, unscented, and provides infrared and blue light protection.*
FDA Label Image

Active Ingredients (Active Ingredients)

Active Ingredients (Active Ingredients)
Drug Facts panel listing the active ingredient Zinc Oxide 12% and its purpose as a sunscreen. The panel is minimal and focused on this ingredient and its function.*
FDA Label Image

Dosage And Administration (Directions)

Dosage And Administration (Directions)
The image displays directions and sun protection measures for topical use, advising to shake well before use, apply liberally 15 minutes before sun exposure, and reapply after swimming, sweating, or towel drying. It includes sun safety tips like limiting sun exposure time and wearing protective clothing, noting children under 6 months should consult a doctor.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
A text panel listing inactive ingredients for Organys Derma Made Zinc Oxide 132 mg/mL topical lotion. Ingredients include various solvents, silicones, emulsifiers, antioxidants, preservatives, and colorants such as water, dimethicone, niacinamide, allantoin, sodium chloride, phenoxyethanol, and iron oxides. No active ingredient information is shown.*
FDA Label Image

Indication And Usage (Uses)

Indication And Usage (Uses)
A partial Drug Facts panel listing the Uses section for a topical product, including that it helps prevent sunburn and decreases the risk of skin cancer and aging when used with other sun protection measures. The text is small and only this section is visible.*
FDA Label Image

Keep Out Of Reach Of Children (Warning)

Keep Out Of Reach Of Children (Warning)
This image shows a warning label panel advising that the product is for external use only, should not be used on damaged or broken skin, and to avoid contact with eyes. It instructs to rinse with water if contact occurs, to stop use and consult a doctor if a skin rash develops, and to keep the product out of reach of children. If swallowed, medical help or Poison Control Center contact is recommended immediately.*

* 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.