Home NDC 69423-850 Crest 3D White
Product NDC 69423-850
11-digit product format 694230850
Labeler code 69423
Product ID 69423-850_47e3b649-b414-5dd2-e063-6294a90a3919
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler The Procter & Gamble Manufacturing Company
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-12-01
Substance SODIUM 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 3D White
Brand name suffix Ultra Vivid Mint
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM 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 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 891775 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 69423-850-52 Crest 3D WhiteUltra Vivid Mint 1 in 1 CARTON PASTE, DENTIFRICE 1 6 69423-850-52 Crest 3D WhiteUltra Vivid Mint 147 g in 1 TUBE PASTE, DENTIFRICE 147 6 69423-850-85 Crest 3D WhiteUltra Vivid Mint 24 g in 1 TUBE PASTE, DENTIFRICE 24 6 69423-850-85 Crest 3D WhiteUltra Vivid Mint 1 in 1 CARTON PASTE, DENTIFRICE 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69423-850 CREST 3D WHITE ULTRA VIVID MINT (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 4 Current NDC, Legacy NDC, 4 package rows 20250110_cba96ef0-0519-059f-e053-2a95a90a43ad.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 6 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 69423-850-52 69423085052 1 TUBE in 1 CARTON (69423-850-52) / 147 g in 1 TUBE 1 tube 2021-12-01 0000-00-00 No No Current 69423-850-85 69423085085 1 TUBE in 1 CARTON (69423-850-85) / 24 g in 1 TUBE 1 tube 2025-08-04 No No Current