Home NDC 69842-218 CVS Restore and Defend Sensitive
Product NDC 69842-218
11-digit product format 698420218
Labeler code 69842
Product ID 69842-218_47e5f657-c061-b740-e063-6394a90a114e
Type HUMAN OTC DRUG
Nonproprietary name Stannous fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler CVS Pharmacy
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-02-11
Substance STANNOUS FLUORIDE
Active strength .454 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 69842-218 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 69842-218 69842-218-19 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 CVS Restore and Defend Sensitive
Brand name suffix Whitening
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength STANNOUS FLUORIDE .454 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3FTR44B32Q Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 416784 Internal RxNorm 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 69842-218-19 CVS Restore and Defend SensitiveWhitening 1 in 1 CARTON PASTE, DENTIFRICE 1 7 69842-218-19 CVS Restore and Defend SensitiveWhitening 96.4 g in 1 TUBE PASTE, DENTIFRICE 96.4 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-218 CVS RESTORE AND DEFEND SENSITIVE WHITENING (STANNOUS FLUORIDE) PASTE, DENTIFRICE [CVS PHARMACY] 6 Current NDC, Legacy NDC, 2 package rows 20250121_81b72da2-7f41-74ca-e053-2a91aa0a9646.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 38 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 Marketing end Sample Exclude flag Status 69842-218-19 69842021819 1 TUBE in 1 CARTON (69842-218-19) / 96.4 g in 1 TUBE 1 tube 2019-02-11 0000-00-00 No No Current