Home NDC 81239-100-02 Baird Good Night
Product NDC 81239-100
Requested package NDC 81239-100-02
11-digit product format 812390100
Labeler code 81239
Product ID 81239-100_bdc38b9d-2e2b-495b-e053-2995a90a215a
Type HUMAN OTC DRUG
Nonproprietary name Sodium fluoride, Sodium monofluorophosphate
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler JK INSPIR Co., Ltd
Application part355
Marketing category OTC MONOGRAPH FINAL
Marketing start 2020-12-03
Marketing end 0000-00-00
Substance SODIUM FLUORIDE; SODIUM MONOFLUOROPHOSPHATE
Active strength 1 g/100g; g/100g
NDC exclude flag No
Listing certified through 2022-12-31
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 · 16 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81239-100-01 Baird Good Night 100 g in 1 TUBE PASTE, DENTIFRICE 100 7 81239-100-02 Baird Good Night 1 in 1 CARTON PASTE, DENTIFRICE 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81239-100 BAIRD GOOD NIGHT (SODIUM FLUORIDE, SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [JK INSPIR CO., LTD] 7 Legacy NDC, 2 package rows 20210319_b5992295-4a53-3930-e053-2a95a90af8e3.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81239-100-02 81239010002 1 TUBE in 1 CARTON (81239-100-02) > 100 g in 1 TUBE (81239-100-01) 1 tube 2020-12-03 0000-00-00 No No Current