Home NDC 67751-124 Crest Cavity Protection Regular
Product NDC 67751-124
11-digit product format 677510124
Labeler code 67751
Product ID 67751-124_2384dc77-0c7e-1373-e063-6394a90a4a65
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Navajo Manufacturing Company Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 1984-08-02
Substance SODIUM FLUORIDE
Active strength 1.5 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
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 Cavity Protection Regular
Listing expiration 2026-12-31 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67751-124-01 Crest Cavity Protection Regular 1 in 1 BLISTER PACK PASTE, DENTIFRICE 1 1 67751-124-01 Crest Cavity Protection Regular 24 g in 1 TUBE PASTE, DENTIFRICE 24 1 67751-124-02 Crest Cavity Protection Regular 24 g in 1 TUBE PASTE, DENTIFRICE 24 1 67751-124-02 Crest Cavity Protection Regular 1 in 1 BLISTER PACK PASTE, DENTIFRICE 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67751-124 CREST CAVITY PROTECTION REGULAR (SODIUM FLUORIDE) PASTE, DENTIFRICE [NAVAJO MANUFACTURING COMPANY INC.] 1 Current NDC, 4 package rows 20241004_23851360-e30e-dd97-e063-6394a90a5474.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 30 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 67751-124-01 67751012401 1 TUBE in 1 BLISTER PACK (67751-124-01) / 24 g in 1 TUBE 1 tube 1999-11-26 No No Current 67751-124-02 67751012402 1 TUBE in 1 BLISTER PACK (67751-124-02) / 24 g in 1 TUBE 1 tube 1999-11-26 No No Current