Seborrheic Dermatitis And Psoriasis
Product Images NDC 81799-007

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Seborrheic Dermatitis And Psoriasis (NDC 81799-007). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ehy Holdings Llc, 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

81799-006-1 1 (81799 005 1 1)

Packaging label for RoyceDerm Herpes Relief Cream, a 2 oz (60g) topical cream. The label features claims of fighting outbreaks, soothing and cooling, and reducing recurrence. Active ingredient is Graphites 1%. Distributed by RoyceDerm LLC, Sheridan, WY. The label includes drug facts, inactive ingredients, directions, warnings, and contact information.*

FDA Label Image

81799-006-1 2 (81799 005 1 2)

Packaging label for RoyceDerm Herpes Relief Cream, a 2 oz (60g) topical cream. The label highlights that the product helps relieve symptoms of rashes, blisters, itching, redness, and pain. It is distributed by RoyceDerm LLC, Sheridan, WY. The active ingredient is Graphites 1%, with a purpose for relief of skin eruptions and itching in the genital area. The label also lists warnings, directions, inactive ingredients, and contact information for customer care.*

FDA Label Image

81799-006-1 3 (81799 005 1 3)

Packaging and tube label for RoyceDerm Herpes Relief Cream, a 2 oz (60 g) topical cream. The label highlights that it helps relieve symptoms of rashes, blisters, itchiness, redness, and pain. It features claims of being all natural and fast acting, and states it fights outbreaks, soothes and cools, and reduces recurrence. The packaging shows molecular graphics with blue and white color schemes.*

* 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.