Allday 5000 Sensitive Paste, Dentifrice
Product Images NDC 57511-0006

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Allday 5000 Sensitive (NDC 57511-0006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Elevate Oral Care, 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

Instructions For Use (Instructions For Use)

This image shows the detailed prescribing information for Allday 5000 Sensitive, a 1.1% sodium fluoride prescription-strength topical toothpaste. The text includes the product description, active and inactive ingredients, clinical pharmacology, indications, contraindications, warnings, precautions, overdosage, dosage and administration, how supplied, and storage instructions.*

FDA Label Image

Primary Package Label (Primary Label)

This image shows detailed medication information and branding for Allday 5000 Sensitive Anticavity Toothpaste with 1.1% Sodium Fluoride, a prescription-strength dental paste by Elevate Oral Care. It includes indications, active ingredients, dosage instructions, warnings, storage details, and promotes its mild mint flavor with 38% xylitol content. Additional products for dry mouth relief by the same brand are also depicted.*

FDA Label Image

Warnings (Warnings)

A drug facts and warning label panel for Allday 5000 Sensitive toothpaste containing 1.1% sodium fluoride. The panel includes warnings about dental fluorosis risk in pediatric patients under 12 years, precautions for use, pregnancy category information, nursing mother advice, pediatric use caution, and overdose guidance including ingestion management.*

* 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.