Home NDC 37000-972-41 Native
Product NDC 37000-972
Requested package NDC 37000-972-41
11-digit product format 370000972
Labeler code 37000
Product ID 37000-972_d60862ce-dc0f-6e2b-e053-2995a90ad495
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Procter & Gamble Manufacturing Company
Application part355
Marketing category OTC MONOGRAPH FINAL
Marketing start 2020-01-01
Marketing end 0000-00-00
Substance SODIUM FLUORIDE
Active strength 1 mg/g
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 · 2 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 37000-972 37000-972-41 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 37000-972 37000-972-41 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37000-972 NATIVE CHARCOAL (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] 6 Legacy NDC 20250110_a52460b4-1bb0-521a-e053-2995a90ad217.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 37000-972-41 37000097241 1 TUBE in 1 CARTON (37000-972-41) > 116 g in 1 TUBE 1 tube 2020-01-01 0000-00-00 No No Current