Home NDC 69423-760 Crest 3D White
Product NDC 69423-760
11-digit product format 694230760
Labeler code 69423
Product ID 69423-760_49ee5903-6e3a-c329-e063-6294a90a3be4
Type HUMAN OTC DRUG
Nonproprietary name Sodium monofluorophosphate
Dosage form PASTE, DENTIFRICE
Route ORAL
Labeler The Procter & Gamble Manufacturing Company
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-01-10
Substance SODIUM MONOFLUOROPHOSPHATE
Active strength 1.7 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 Brilliance Pro Ultra White
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM MONOFLUOROPHOSPHATE 1.7 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C810JCZ56Q Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1038995 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 69423-760-30 Crest 3D WhiteBrilliance Pro Ultra White 1 in 1 CARTON PASTE, DENTIFRICE 1 9 69423-760-30 Crest 3D WhiteBrilliance Pro Ultra White 85 g in 1 TUBE PASTE, DENTIFRICE 85 9 69423-760-38 Crest 3D WhiteBrilliance Pro Ultra White 107 g in 1 TUBE PASTE, DENTIFRICE 107 9 69423-760-38 Crest 3D WhiteBrilliance Pro Ultra White 1 in 1 CARTON PASTE, DENTIFRICE 1 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69423-760 CREST 3D WHITE BRILLIANCE PRO ULTRA WHITE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 7 Current NDC, 4 package rows 20250227_f4c02924-95ee-09d2-e053-2995a90a8121.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 Sample Exclude flag Status 69423-760-30 69423076030 1 TUBE in 1 CARTON (69423-760-30) / 85 g in 1 TUBE 1 tube 2023-01-10 No No Current 69423-760-38 69423076038 1 TUBE in 1 CARTON (69423-760-38) / 107 g in 1 TUBE 1 tube 2023-01-10 No No Current