Home NDC 70108-204 evo ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT
Product NDC 70108-204
11-digit product format 701080204
Labeler code 70108
Product ID 70108-204_24b40856-ae7e-4c3c-b559-6e5855b22506
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Ashtel Studios, Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-30
Marketing end 2028-03-29
Substance SODIUM FLUORIDE
Active strength .24 g/100g
NDC exclude flag No
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base evo ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .24 g/100g
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70108-204-01 evo ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT 1 in 1 BOX PASTE, DENTIFRICE 1 1 70108-204-01 evo ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT 99 g in 1 TUBE PASTE, DENTIFRICE 99 1
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 33 of 50 · 995 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70108-204-01 70108020401 1 TUBE in 1 BOX (70108-204-01) / 99 g in 1 TUBE 1 tube 2025-06-30 2028-03-29 No No Historical