Home NDC 87536-001 SensitiveToothpaste
Product NDC 87536-001
11-digit product format 875360001
Labeler code 87536
Product ID 87536-001_4db239f3-2ad8-3a5b-e063-6294a90a11a7
Type HUMAN OTC DRUG
Nonproprietary name Anti sensitiveToothpaste
Dosage form PASTE, DENTIFRICE
Route SUBGINGIVAL
Labeler Huain Best Trade Co., Ltd.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-23
Substance POTASSIUM NITRATE
Active strength 5 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 SensitiveToothpaste
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM NITRATE 5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination RU45X2JN0Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87536-001-01 SensitiveToothpaste 1 g 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 5 of 50 · 995 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87536-001-01 87536000101 1 g in 1 BOX (87536-001-01) 1 g 2026-03-23 No No Current