Barmicil Plus Cream
Product Images NDC 69729-834

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 Barmicil Plus (NDC 69729-834). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Opmx 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

Pdp Interior (Pdp Int)

Pdp Interior (Pdp Int)
Packaging label for Barmicil Plus Hydrocortisone cream 10 mg/g, topical use, labeled in Spanish. The label includes medication data, active ingredient, uses, warnings, indications, inactive ingredients, storage instructions, and contact information. The labeler is OPMX LLC and the product is an over-the-counter human drug.*
FDA Label Image

Top Pdp (Pdp Tube)

Top Pdp (Pdp Tube)
Barmicil Plus 1% Hydrocortisone Anti-Itch Cream with Aloe Vera, 1 oz (28 g) topical cream. The label highlights 'Maximum Strength Cream' and includes usage instructions, warnings, and active ingredient details. The product is labeled for temporary relief of itching associated with minor skin irritations. Manufactured by RRx, San Diego, CA, and distributed by OPMX LLC, Chula Vista, CA. Made in India.*
FDA Label Image

Pdp (Pdp)

Pdp (Pdp)
Packaging label for Barmicil Plus cream with Aloe Vera, containing 1% Hydrocortisone as the active ingredient. This maximum strength topical cream comes in a 1 oz (28 g) tube. It is labeled as an anti-itch cream for external use. The label includes drug facts, warnings, directions, inactive ingredients, and manufacturer information for OPMX LLC, San Diego, CA.*

* 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.