Ultrasolsunscreen
Product Images NDC 59886-322

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Ultrasolsunscreen (NDC 59886-322). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fischer Pharmaceuticals Ltd, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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FDA Label Image

Pdp And Back (67069 Lotion)

Pdp And Back (67069 Lotion)
This is a description of Dr. Fischer Ultras Sunscreen Lotion, which provides broad spectrum UVA and UVB protection. The lotion is hypoallergenic and is recommended by dermatologists. It contains active ingredients such as avobenzone, octinoxate, octisalate, and oxybenzone. The lotion retains SPF after 80 minutes of water activity or sweating. The instruction is to apply generously to all exposed areas before sun exposure and reapply as needed. The lotion is not recommended for children under the age of 6 months. It is also warned to avoid eye contact and not to swallow the lotion. If rash or irritation develops and lasts, stop use and ask a doctor. If swallowed, get medical help. The product information suggests that limiting sun exposure, using protective clothing, and applying sunscreen may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun. Some fabrics may stain when in contact with the lotion. The lotion is manufactured by Fischer Pharmaceuticals Ltd. in Israel.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.