Home NDC 69968-0819 Listerine Clinical Solutions Teeth Strength Alpine Mint
Product NDC 69968-0819
11-digit product format 699680819
Labeler code 69968
Product ID 69968-0819_223b617c-b851-5b58-e063-6394a90a57b0
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form MOUTHWASH
Route ORAL
Labeler Kenvue Brands LLC
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-10-16
Substance SODIUM FLUORIDE
Active strength .1 mg/mL
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 Listerine Clinical Solutions Teeth Strength Alpine Mint
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .1 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 313029 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69968-0819-1 Listerine Clinical Solutions Teeth Strength Alpine Mint 1000 mL in 1 BOTTLE MOUTHWASH 1000 3 69968-0819-5 Listerine Clinical Solutions Teeth Strength Alpine Mint 500 mL in 1 BOTTLE MOUTHWASH 500 3 69968-0819-9 Listerine Clinical Solutions Teeth Strength Alpine Mint 95 mL in 1 BOTTLE MOUTHWASH 95 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0819 LISTERINE CLINICAL SOLUTIONS TEETH STRENGTH ALPINE MINT (SODIUM FLUORIDE) MOUTHWASH [KENVUE BRANDS LLC] 3 Current NDC, 3 package rows 20241114_06e2de03-4a58-3de0-e063-6294a90a5857.zip
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69968-0819-1 69968081901 1000 mL in 1 BOTTLE (69968-0819-1) 1000 ml 2023-10-16 No No Current 69968-0819-5 69968081905 500 mL in 1 BOTTLE (69968-0819-5) 500 ml 2023-10-16 No No Current 69968-0819-9 69968081909 95 mL in 1 BOTTLE (69968-0819-9) 95 ml 2023-10-16 No No Current