IODENT SENSITIVE

Product NDC: 72129-002
Requested package NDC: 72129-002-01
11-digit product format: 721290002
Labeler code: 72129
Product ID: 72129-002_d80b4544-0e75-218b-e053-2a95a90a5005
Type: HUMAN OTC DRUG
Nonproprietary name: Potassium Nitrate,Sodium Fluoride
Dosage form: PASTE
Route: DENTAL
Labeler: Zhaoqing Longda Biotechnology Co., Ltd.
Application: part356
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2018-02-02
Marketing end: 0000-00-00
Substance: POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength: 5 g/100g; g/100g
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	72129-002	72129-002-01	I	Inactivated by FDA		2026-10-05

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 · 18 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…`
2021-12-27 23:28 UTC · source 2021-12-27	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	`9bebd1f3094a…`	`5416666fcb17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72129-002-01	2023-07-28	C162847	48780-1	9d75b9d0-c1e1-f424-e053-dadaa90a57ce	72129 002 Potassium Nitrate Sodium Fluoride
72129-002-01	2022-02-15	C162847	48780-1	9d75b9d0-c1e1-f424-e053-dadaa90a57ce	72129 002 Potassium Nitrate Sodium Fluoride
72129-002-01	2020-01-31	C162847	48780-1	9d75b9d0-c1e1-f424-e053-dadaa90a57ce	72129 002 Potassium Nitrate Sodium Fluoride

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72129-002-01	IODENT SENSITIVE	24 in 1 BOX	PASTE	24		2
72129-002-01	IODENT SENSITIVE	12 in 1 PACKAGE	PASTE	12		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72129-002	IODENT SENSITIVE (POTASSIUM NITRATE,SODIUM FLUORIDE) PASTE [ZHAOQING LONGDA BIOTECHNOLOGY CO., LTD.]	2	Legacy NDC, 2 package rows	20220216_65ce884d-8106-30ac-e053-2991aa0ab486.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
RU45X2JN0Z	POTASSIUM NITRATE	7757-79-1	POTASSIUM NITRATE
8ZYQ1474W7	SODIUM FLUORIDE	7681-49-4	SODIUM FLUORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1038841	potassium nitrate 5 % / sodium fluoride 0.15 % Toothpaste	PSN	65ce884d-8106-30ac-e053-2991aa0ab486	2
1038841	potassium nitrate 0.05 MG/MG / sodium fluoride 0.0015 MG/MG Toothpaste	SCD	65ce884d-8106-30ac-e053-2991aa0ab486	2
1038841	K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0015 MG/MG Toothpaste	SY	65ce884d-8106-30ac-e053-2991aa0ab486	2
1038841	pot nitrate 0.05 MG/MG / sodium fluoride 0.0015 MG/MG gel Toothpaste	SY	65ce884d-8106-30ac-e053-2991aa0ab486	2
1038841	Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0015 MG/MG Toothpaste	SY	65ce884d-8106-30ac-e053-2991aa0ab486	2
1038841	potassium nitrate 5 % / sodium fluoride 0.15 % Toothpaste	SY	65ce884d-8106-30ac-e053-2991aa0ab486	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72129-002-01	72129000201	24 PACKAGE in 1 BOX (72129-002-01) > 12 TUBE in 1 PACKAGE > 113 g in 1 TUBE	24 package	2018-02-02	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
72129 002 Potassium Nitrate Sodium Fluoride	Zhaoqing Longda Biotechnology Co., Ltd.	2022-02-15	HUMAN OTC DRUG LABEL	2