Hydrocortisone Cream
Product Images NDC 0168-0015

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 0168-0015). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by E. Fougera & Co. A Division Of Fougera Pharmaceuticals, 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

Structural Formula (Hyd0b 0002 01)

Structural Formula (Hyd0b 0002 01)
Chemical structure diagram of hydrocortisone, showing its steroid framework with functional groups including hydroxyl and carbonyl groups.*
FDA Label Image

Tube (Hyd0b 0002 02)

Tube (Hyd0b 0002 02)
Label for Hydrocortisone Cream USP, 1% (10 mg/g) topical cream by E. Fougera & Co., a division of Fougera Pharmaceuticals, LLC. The label states the product is for external use only, not for ophthalmic use, with a net weight of 28.35 g (1 oz). Instructions mention 2 to 3 applications daily, storage at 15° to 30°C, and a puncture seal on the cap. Ingredients include hydrocortisone and excipients such as glyceryl monostearate and petrolatum.*
FDA Label Image

Carton (Hyd0b 0002 03)

Carton (Hyd0b 0002 03)
Packaging label for Hydrocortisone Cream USP, 1% (10 mg/g) topical cream. The label indicates external use only and not for ophthalmic use. It includes directions for application, storage instructions, and a list of inactive ingredients. The product is labeled by E. Fougera & Co., a division of Fougera Pharmaceuticals, LLC, with a net weight of 28.35 g (1 oz). Barcode and NDC 0168-0015-31 are also visible.*

* 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.