Home NDC 10237-632 Aim Sensitive
Product NDC 10237-632
11-digit product format 102370632
Labeler code 10237
Product ID 10237-632_9376e043-f45a-5c1f-e053-2a95a90ac1ce
Type HUMAN OTC DRUG
Nonproprietary name Potassium nitrate, Sodium Fluoride
Dosage form GEL, DENTIFRICE
Route DENTAL
Labeler Church & Dwight Co., Inc.
Application part356
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2015-03-25
Marketing end 0000-00-00
Substance POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength 50 mg/g; mg/g
NDC exclude flag No
Listing certified through 2020-12-31
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 · 31 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 10237-632-55 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 10237-632-55 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 10237-632-55 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 10237-632-55 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 10237-632-55 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 10237-632-55 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product D Discontinued by firm 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 10237-632-55 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 10237-632-55 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 10237-632-55 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 10237-632-55 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 10237-632-55 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 10237-632-55 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded POTASSIUM NITRATE ACTIVE INGREDIENT RU45X2JN0Z AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 SODIUM FLUORIDE ACTIVE INGREDIENT 8ZYQ1474W7 AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 FLUORIDE ION ACTIVE MOIETY Q80VPU408O AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 NITRATE ION ACTIVE MOIETY T93E9Y2844 AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM INACTIVE INGREDIENT K679OBS311 AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 D&C RED NO. 33 INACTIVE INGREDIENT 9DBA0SBB0L AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 HYDRATED SILICA INACTIVE INGREDIENT Y6O7T4G8P9 AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 POLYETHYLENE GLYCOL 400 INACTIVE INGREDIENT B697894SGQ AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R AIM SENSITIVE CAVITY PROTECTION (POTASSIUM NITRATE, SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] 1