Home NDC 0135-5025 SENSODYNE
Product NDC 0135-5025
11-digit product format 001355025
Labeler code 0135
Product ID 0135-5025_13123f95-ce72-c317-e063-6394a90ac2d2
Type HUMAN OTC DRUG
Nonproprietary name stannous fluoride
Dosage form PASTE
Route ORAL
Labeler Haleon US Holdings LLC
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-06
Substance STANNOUS FLUORIDE
Active strength 1.1 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base SENSODYNE
Brand name suffix SENSITIVITY AND GUM CLEAN AND FRESH
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength STANNOUS FLUORIDE 1.1 mg/g
Harmonized Identifiers# Field, Values table Field Values Unii 3FTR44B32Q Rxcui 416784
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0135-5025-01 SENSODYNESENSITIVITY AND GUM CLEAN AND FRESH 96.4 g in 1 TUBE PASTE 96.4 6 0135-5025-01 SENSODYNESENSITIVITY AND GUM CLEAN AND FRESH 1 in 1 CARTON PASTE 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0135-5025 SENSODYNE SENSITIVITY AND GUM MINT (STANNOUS FLUORIDE) PASTE SENSODYNE SENSITIVITY AND GUM WHITENING (STANNOUS FLUORIDE) PASTE SENSODYNE SENSITIVITY AND GUM CLEAN AND FRESH (STANNOUS FLUORIDE) PASTE [HALEON US HOLDINGS LLC] 6 Current NDC, Legacy NDC, 2 package rows 20240308_ed093acd-255c-40ff-a010-d276f5844453.zip
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 0135-5025-01 00135502501 1 TUBE in 1 CARTON (0135-5025-01) / 96.4 g in 1 TUBE 1 tube 2021-01-06 0000-00-00 No No Current