Hydrocortisone Cream
Product Images NDC 61010-5800

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydrocortisone (NDC 61010-5800). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safetec Of America, Inc., 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

Saf0a 0003 01

Saf0a 0003 01
Drug Facts panel for 1% Hydrocortisone Cream 0.9 g by Safetec of America, Inc. Details active ingredient hydrocortisone 1.0% as anti-itch, uses for temporary relief of itching from minor skin irritation, warnings for external use only, and directions for application up to 3 to 4 times daily. Also includes stop use warnings, keeping out of reach of children, and a list of inactive ingredients like emulsifying wax, ethanol, mineral oil, and others.*
FDA Label Image

Saf0a 0003 02

Saf0a 0003 02
Box packaging for Safetec First Aid 1% Hydrocortisone Cream, a topical OTC drug for temporary relief of itching from minor skin irritations, inflammation, or rashes. The label states it contains 144 packets, each 0.9g. Manufacturer and contact details for Safetec of America, Inc. are included, along with drug facts and directions for use.*
FDA Label Image

Saf0a 0003 03

Saf0a 0003 03
The image shows a carton label for Safetec First Aid Hydrocortisone Cream, 1% strength (10 mg/g), topical cream. The label indicates 10 individual packets, each containing 0.9g of cream. The packaging emphasizes relief from itching, inflammation, and rashes. The label includes Drug Facts with active ingredient, uses, warnings, directions, other information, and a list of inactive ingredients.*

* 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.