Quadriderm Nf Cream
Product Images NDC 69729-828

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 Quadriderm Nf (NDC 69729-828). 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

Esp (Quadriderm Nf Esp)

Esp (Quadriderm Nf Esp)
This panel provides drug facts for Quadriderm NF 10 mg/g topical cream with the active ingredient hydrocortisone. It includes information on usage for relief of itching, anti-itch effects, inactive ingredients, storage instructions, warnings for external use only, and directions for application in adults and children. It also advises consulting a doctor for children under 12 and details on when to stop use or seek medical advice.*
FDA Label Image

Pdp (Quadriderm Nf Pdp)

Pdp (Quadriderm Nf Pdp)
Packaging label for Quadriderm NF 1% Hydrocortisone with Aloe Vera Anti-Itch Cream, topical cream in a 2 oz (56 g) tube. Label highlights its use for itch relief and lists conditions such as inflammation, redness, skin irritation, rashes, insect bites, poison ivy, eczema, and psoriasis. Manufactured and distributed by OPMX LLC.*
FDA Label Image

Tube (Quadriderm Tube)

Tube (Quadriderm Tube)
Quadriderm NF 1% Hydrocortisone Anti-Itch Cream in a 56g (2 oz) tube. The label highlights it as maximum strength and notes it contains Aloe Vera. Manufactured by OPMX LLC, Chula Vista, CA. The label includes directions, warnings, inactive ingredients, and contact information for questions or comments.*

* 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.