Home NDC 87118-003 Seavue Dental Desensitizer
Product NDC 87118-003
11-digit product format 871180003
Labeler code 87118
Product ID 87118-003_3f47f399-1a15-5264-e063-6394a90aeb1c
Type HUMAN OTC DRUG
Nonproprietary name potassium nitrate and sodium fluoride dentifrice
Dosage form GEL, DENTIFRICE
Route DENTAL
Labeler Xiling (Zhenjiang) Medical Technology Co., Ltd.
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-08
Substance SODIUM FLUORIDE; POTASSIUM NITRATE
Active strength 1.36; 26 mg/g; mg/g
NDC exclude flag No
Listing certified through 2026-12-31
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 Seavue Dental Desensitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 1.36 mg/g POTASSIUM NITRATE 26 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup 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 87118-003-01 Seavue Dental Desensitizer 1 g in 1 BOX GEL, 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 9 of 40 · 786 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87118-003-01 87118000301 1 g in 1 BOX (87118-003-01) 1 g 2025-10-08 No No Current