Home NDC 69423-875 Crest
Product NDC 69423-875
11-digit product format 694230875
Labeler code 69423
Product ID 69423-875_47e495e8-478e-b045-e063-6294a90a438e
Type HUMAN OTC DRUG
Nonproprietary name Stannous fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler The Procter & Gamble Manufacturing Company
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-01-01
Substance STANNOUS FLUORIDE
Active strength 1.5 mg/g
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 Crest
Brand name suffix Densify Daily Whitening
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength STANNOUS FLUORIDE 1.5 mg/g
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69423-875-41 CrestDensify Daily Whitening 1 in 1 CARTON PASTE, DENTIFRICE 1 6 69423-875-41 CrestDensify Daily Whitening 116 g in 1 TUBE PASTE, DENTIFRICE 116 6 69423-875-53 CrestDensify Daily Whitening 1 in 1 CARTON PASTE, DENTIFRICE 1 6 69423-875-53 CrestDensify Daily Whitening 150 g in 1 TUBE PASTE, DENTIFRICE 150 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69423-875 CREST DENSIFY DAILY WHITENING (STANNOUS FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 5 Current NDC, Legacy NDC, 4 package rows 20250227_d811306f-4994-7a5a-e053-2995a90adf16.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 22 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 69423-875-41 69423087541 1 TUBE in 1 CARTON (69423-875-41) / 116 g in 1 TUBE 1 tube 2022-01-01 0000-00-00 No No Current 69423-875-53 69423087553 1 TUBE in 1 CARTON (69423-875-53) / 150 g in 1 TUBE 1 tube 2022-01-01 No No Current