Home NDC 57511-0504-01 NDC 57511-0504-01 - FluoriMax 5000 This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 57511-0504
Requested NDC 57511-0504-01
Package NDCs from labels 57511-0504-1, 57511-0504-2, 57511-0504-01
Manufacturer Elevate Oral Care
Effective date 2025-09-19
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57511-0504-1 FluoriMax 5000 96 g in 1 TUBE PASTE, DENTIFRICE 96 2 57511-0504-2 FluoriMax 5000 2 in 1 BOX PASTE, DENTIFRICE 2 2 57511-0504-1 FluoriMax 5000 96 g in 1 TUBE PASTE, DENTIFRICE 96 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57511-0504 FLUORIMAX 5000 (1.1% SODIUM FLUORIDE TOOTHPASTE) PASTE, DENTIFRICE [ELEVATE ORAL CARE] 1 Current NDC, Legacy NDC, 2 package rows 20220615_d9e462d9-f0fd-4168-e053-2995a90a95b2.zip 57511-0504 FLUORIMAX 5000 (1.1% SODIUM FLUORIDE TOOTHPASTE) PASTE, DENTIFRICE [ELEVATE ORAL CARE] 1 Current NDC, Legacy NDC, 1 package rows 20200902_ae45ae2d-a21f-0a05-e053-2995a90a4d5e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 5 of 70 · 1,396 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.