Biobarrier Renewal Cream
Product Images NDC 72203-019

View Photos of 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 Biobarrier Renewal Cream (NDC 72203-019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluemercury, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Biobarrier Tube (Bm M61 Biobarrier Renewalcream Component 011624 Final)

Biobarrier Tube (Bm M61 Biobarrier Renewalcream Component 011624 Final)
Label design for BioBarrier Renewal Cream by bluemercury, containing 0.75% allantoin in a 1.7 oz (50 g) topical cream. The front features the product name and description highlighting triple ceramide and allantoin cushion cream, while the back includes active ingredient details, directions, cautions, and manufacturer information. The label has a dark purple background with white text and includes gluten-free and vegan icons.*
FDA Label Image

Biobarrier Renewal Cream Carton (Bm M61 M61s02 Biobarrier Renewalcream Carton 011624 Final)

Biobarrier Renewal Cream Carton (Bm M61 M61s02 Biobarrier Renewalcream Carton 011624 Final)
Label artwork for BioBarrier Renewal Cream by bluemercury, featuring m-61 powerful skincare branding. The cream contains 7.5 mg/g allantoin as the active ingredient. The label lists the product as a renewing nutrient-rich triple ceramide and allantoin cushion cream for topical use. The package size is 1.7 oz (50 g). The label includes drug facts, directions, inactive ingredients, a barcode, and various certifications and logos.*

* 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.