Home NDC 84126-675 Crest
Product NDC 84126-675
11-digit product format 841260675
Labeler code 84126
Product ID 84126-675_5ed7b9c1-5a3d-6c02-e063-6294a90a0ca2
Type HUMAN OTC DRUG
Nonproprietary name Sodium monofluorophosphate
Dosage form KIT
Route ORAL
Labeler The Procter & Gamble Manufacturing Company
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-09-15
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 New Year New Smile
Listing expiration 2027-12-31 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.
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 31 of 48 · 950 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84126-675-01 84126067501 1 KIT in 1 CARTON (84126-675-01) * 59 g in 1 TUBE (84126-611-01) 1 kit 2026-09-15 No No Current