Home NDC 69968-0687 Listerine Smart Rinse Anticavity Fluoride Rinse - Berry Splash
Product NDC 69968-0687
11-digit product format 699680687
Labeler code 69968
Product ID 69968-0687_22c5f4a1-b570-be23-e063-6394a90a9bbf
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 2021-01-01
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 Smart Rinse Anticavity Fluoride Rinse - Berry Splash
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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 313029 Internal RxNorm lookup 1798474 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 69968-0687-5 Listerine Smart Rinse Anticavity Fluoride Rinse - Berry Splash 500 mL in 1 BOTTLE MOUTHWASH 500 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0687 LISTERINE SMART RINSE ANTICAVITY FLUORIDE RINSE - BERRY SPLASH (SODIUM FLUORIDE) MOUTHWASH [KENVUE BRANDS LLC] 4 Current NDC, Legacy NDC, 1 package rows 20241114_ee9a962d-83c7-4b13-bff6-140e48785e8a.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 33 of 49 · 972 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 69968-0687-5 69968068705 500 mL in 1 BOTTLE (69968-0687-5) 500 ml 2021-01-01 0000-00-00 No No Current