Decure Paste, Dentifrice
Product Images NDC 84132-100

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Decure (NDC 84132-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Scope Medical Devices Private Limited, 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

Principal Display Panel (53 mL Bottle Label)

Drug Facts panel for Instant Hand Antiseptic contains 70.0% ethyl alcohol per 100ml, intended for hand sanitization to decrease skin bacteria. Warnings include flammability and advice for external use only. Directions specify supervision for children under 6 and avoiding contact with eyes. Additional information includes storage instructions, ingredients, and distributor details from ASP Global LLC.*

FDA Label Image

Principal Display Panel (10 gm Tube Label)

Drug Facts panel from Decure toothpaste containing Sodium Monofluorophosphate 0.76% as the active ingredient for anticavity purposes. The text includes uses, warnings, directions for use in adults and children, and a list of inactive ingredients. It also features manufacturing details and a barcode.*

FDA Label Image

Principal Display Panel (Kit Label)

Northside Hospital Maternity Backpack BASE kit featuring a grey maternity backpack with front, back, and top views showing multiple compartments and shoulder straps. A smaller zippered pouch containing four labeled travel-size bottles is also included. The kit contains essentials such as sanitary pads, a knit brief, portable bidet, amenity kit case, insulated bottle bag kit, and a spiral hair tie. Labeler is Alliance Formulations.*

* 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.