Home NDC 69423-888-16 ARC
Product NDC 69423-888
Requested package NDC 69423-888-16
11-digit product format 694230888
Labeler code 69423
Product ID 69423-888_dae32c29-cf6a-1eb4-e053-2995a90a787a
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form RINSE
Route ORAL
Labeler The Procter & Gamble Manufacturing Company
Application part355
Marketing category OTC MONOGRAPH FINAL
Marketing start 2021-06-01
Marketing end 0000-00-00
Substance SODIUM FLUORIDE
Active strength 0 mg/mL
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 69423-888 69423-888-16 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
DailyMed Product Concepts# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69423-888 ARC AFTER WHITENING RINSE (SODIUM FLUORIDE) RINSE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 6 Legacy NDC 20250116_dad50805-dd1a-fc0b-e053-2995a90a1bb8.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69423-888-16 69423088816 475 mL in 1 BOTTLE, PLASTIC (69423-888-16) 475 ml 2021-06-01 0000-00-00 No No Current