Hydrocortisone Cream
Product Images NDC 51672-5330

2 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hydrocortisone (NDC 51672-5330). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Carton (Hydrocortisone Aloe Gdv Carton)

Carton (Hydrocortisone Aloe Gdv Carton)
Packaging label for Hydrocortisone Cream 1% topical anti-itch cream with soothing aloe, marketed as providing fast itch relief lasting for hours. The label shows a 1 oz (28.4 g) tube, with branding that compares the active ingredient to Cortizone-10. The product is labeled as maximum strength and distributed by Taro Pharmaceuticals U.S.A., Inc.*
FDA Label Image

Carton (Gdv Hydrocortisone Aloe Ohm Carton)

Carton (Gdv Hydrocortisone Aloe Ohm Carton)
Packaging label for Hydrocortisone Cream 1% with Aloe by Ohm Laboratories, a Sun Pharma company. The label highlights hydrocortisone as an anti-itch topical cream with soothing aloe, marketed as maximum strength for fast itch relief lasting hours. The net weight is 1 oz (28.4 g). It includes usage indications for rash, inflammation, and minor skin irritations. The label references similarity to the active ingredient in Cortizone-10 and shows distribution by Ohm Laboratories Inc., manufactured in India. A barcode and typical drug facts panel 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.