Home NDC 69423-848 Crest Pro-Health Advanced
Product NDC 69423-848
11-digit product format 694230848
Labeler code 69423
Product ID 69423-848_47e52a01-73d0-9fa8-e063-6294a90a018e
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form RINSE
Route ORAL
Labeler The Procter & Gamble Manufacturing Company
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-31
Substance SODIUM FLUORIDE
Active strength 2.2 mg/10mL
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 Pro-Health Advanced
Brand name suffix Anti-Cavity Max Cavity
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 2.2 mg/10mL
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 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 69423-848-01 Crest Pro-Health AdvancedAnti-Cavity Max Cavity 1000 mL in 1 BOTTLE RINSE 1000 5 69423-848-10 Crest Pro-Health AdvancedAnti-Cavity Max Cavity 100 mL in 1 BOTTLE RINSE 100 5 69423-848-21 Crest Pro-Health AdvancedAnti-Cavity Max Cavity 1000 mL in 1 BOTTLE RINSE 1000 5 69423-848-21 Crest Pro-Health AdvancedAnti-Cavity Max Cavity 2 in 1 CELLO PACK RINSE 2 5 69423-848-50 Crest Pro-Health AdvancedAnti-Cavity Max Cavity 500 mL in 1 BOTTLE RINSE 500 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69423-848 CREST PRO-HEALTH ADVANCED ANTI-CAVITY MAX CAVITY (SODIUM FLUORIDE) RINSE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 2 Current NDC, 5 package rows 20250116_15d70b80-3b25-bc32-e063-6394a90a163e.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69423-848-01 69423084801 1000 mL in 1 BOTTLE (69423-848-01) 1000 ml 2020-01-31 No No Current 69423-848-10 69423084810 100 mL in 1 BOTTLE (69423-848-10) 100 ml 2020-01-31 No No Current 69423-848-21 69423084821 2 BOTTLE in 1 CELLO PACK (69423-848-21) / 1000 mL in 1 BOTTLE 2 bottle 2025-07-01 No No Current 69423-848-50 69423084850 500 mL in 1 BOTTLE (69423-848-50) 500 ml 2020-01-31 No No Current