Home NDC 70108-254-01 evo SENSITIVE ANTI-CAVITY FLUORIDE SWEET MINT
Product NDC 70108-254
Requested package NDC 70108-254-01
11-digit product format 701080254
Labeler code 70108
Product ID 70108-254_7d6234e9-f750-4688-8dc6-efcd5089922b
Type HUMAN OTC DRUG
Nonproprietary name Potassium Nitrate, Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Ashtel Studios, Inc.
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-01
Marketing end 2028-04-12
Substance POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength 5; .24 g/100g; 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 SENSITIVE ANTI-CAVITY FLUORIDE SWEET MINT Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM NITRATE 5 g/100g SODIUM FLUORIDE .24 g/100g
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70108-254-01 evo SENSITIVE ANTI-CAVITY FLUORIDE SWEET MINT 99 g in 1 TUBE PASTE, DENTIFRICE 99 1 70108-254-01 evo SENSITIVE ANTI-CAVITY FLUORIDE SWEET MINT 1 in 1 BOX PASTE, DENTIFRICE 1 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 29 of 40 · 782 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 70108-254-01 70108025401 1 TUBE in 1 BOX (70108-254-01) / 99 g in 1 TUBE 1 tube 2025-10-01 2028-04-12 No No Historical