Cerave Developed With Dermatologists Itch Relief Moisturizing Cream
Product Images NDC 49967-512

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 Cerave Developed With Dermatologists Itch Relief Moisturizing (NDC 49967-512). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by L'oreal Usa Products 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

Image Of A Label (Cvircream2)

Image Of A Label (Cvircream2)
Partial Drug Facts label for CeraVe Developed with Dermatologists Itch Relief Moisturizing Cream (pramoxine hydrochloride 10 mg/g) covering warnings about symptoms lasting more than 7 days, usage cautions, and the directions for adults and children. It also lists inactive ingredients including water, glycerin, petrolatum, shea butter, cetyl alcohol, stearic acid, and others.*
FDA Label Image

Image Of A Label (Cvircream3)

Image Of A Label (Cvircream3)
Continuation of the Drug Facts panel for CeraVe Developed with Dermatologists Itch Relief Moisturizing Cream, listing inactive ingredients such as sodium lauroyl lactylate, disodium EDTA, and others. Also includes contact information with a toll-free number and website, trademark and patent details, a statement that the package is free of phthalates, manufacturer information, and country of origin (Made in USA).*
FDA Label Image

Image Of A Label (Cvircreampdp)

Image Of A Label (Cvircreampdp)
Label for CeraVe Developed with Dermatologists Itch Relief Moisturizing Cream containing pramoxine hydrochloride 1% topical cream, 12 oz (340 g). The product is steroid-free and approved by the National Eczema Association. It is indicated for relief of itch and irritation from dry skin, insect bites, and sunburn. The label includes highlights from a clinical study and a Drug Facts panel with active ingredient, use, and warnings. L'Oreal USA Products Inc is the labeler.*

* 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.