Truguard 5000 Paste, Dentifrice
Product Images NDC 71347-500

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Truguard 5000 (NDC 71347-500). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Atlanta Dental Supply Company Dba Advanced Dental Products, 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

Trugrd Box-inner (Trugrd Box Iinner)

TruGuard 5000 Sodium Fluoride Prescription Dental Cream packaging label. The label includes prescribing information, active ingredient details, dosage instructions, warnings, and storage conditions for this human prescription drug toothpaste paste. Labeler is The Atlanta Dental Supply Company DBA Advanced Dental Products. Product NDC is 71347-500.*

FDA Label Image

Trugrd Box-outer (Trugrd Box Outer)

Packaging label for TruGuard 5000 sodium fluoride toothpaste, 1.1% paste dentifrice, 4 oz (112 g) tube. The label emphasizes professional cleaning, contains xylitol to reduce dry mouth, and fresh mint flavor. It is manufactured by The Atlanta Dental Supply Company DBA Advanced Dental Products and is marked for prescription use only.*

FDA Label Image

Tube Label Trugrd (Tube Label Trugrd)

TruGuard 5000 Sodium Fluoride Toothpaste paste in a 4 oz (112 g) tube by The Atlanta Dental Supply Company DBA Advanced Dental Products. The label highlights 1.1% neutral sodium fluoride and potassium nitrate as active ingredients, with flavor described as fresh mint and containing xylitol. It includes drug facts such as indications, warnings, and directions for use. The product is Rx only and intended for professional cleaning systems.*

* 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.