Sensitive Mint Tooth-paste

Product NDC: 79481-0009
11-digit product format: 794810009
Labeler code: 79481
Product ID: 79481-0009_32bc65d7-a30b-44e9-b643-984d3a631de5
Type: HUMAN OTC DRUG
Nonproprietary name: Potassium nitrate, Sodium fluoride
Dosage form: PASTE, DENTIFRICE
Route: DENTAL
Labeler: Meijer, Inc.
Application: M022
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-12-24
Substance: POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength: 50; 2.43 mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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, 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		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	79481-0009-1	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	79481-0009-1	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	79481-0009-1	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	79481-0009-1	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	79481-0009-1	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	79481-0009-1	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	79481-0009-1	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	79481-0009-1	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	79481-0009-1	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Sensitive Mint Tooth-paste
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
POTASSIUM NITRATE	50 mg/g
SODIUM FLUORIDE	2.43 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
RU45X2JN0Z	Internal UNII lookup
8ZYQ1474W7	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1038929	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1e5e8b24-8304-482c-ae80-73effcc345da	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717
6084a4f4-5437-c9a5-caec-5361ee075a59	Product name	1	20140508
90c5639a-61b0-88d6-ddcf-21888e94869a	Product name	1	20140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79481-0009-1	2025-12-24	C162847	48780-1	2cef2736-92dc-d83d-e063-dadaa90ab31f	meijer® sensitive toothpaste FRESH MINT
79481-0009-1	2025-01-30	C162847	48780-1	2cef2736-92dc-d83d-e063-dadaa90ab31f	meijer® sensitive toothpaste FRESH MINT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79481-0009-1	Sensitive Mint Tooth-paste	113 g in 1 TUBE	PASTE, DENTIFRICE	113		4
79481-0009-1	Sensitive Mint Tooth-paste	1 in 1 BOX	PASTE, DENTIFRICE	1		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79481-0009	SENSITIVE MINT TOOTH-PASTE (POTASSIUM NITRATE, SODIUM FLUORIDE) PASTE, DENTIFRICE [MEIJER, INC.]	3	Current NDC, Legacy NDC, 2 package rows	20230112_1e5e8b24-8304-482c-ae80-73effcc345da.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 13 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
S.T.37	HEXYLRESORCINOL	NUMARK BRANDS, INC	7d7acca2-aa8a-5272-e813-faab039cc798	2025-12-15	Warnings	Exact identifier application number: M022
Esunix Oral Bacteriostatic Gel	CETYLPYRIDINIUM CHLORIDE	Xiling (Zhenjiang) Medical Technology Co., Ltd.	3f4ee467-8142-8cb7-e063-6394a90aa7f7	2025-12-12	Warnings	Exact identifier application number: M022
Orajel 4X Medicated For Toothache and Gum	BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	999851ac-925c-7d1f-e053-2a95a90a240b	2025-12-12	Warnings	Exact identifier application number: M022
Orajel 3X Medicated For Toothache and Gum	BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	99a2b061-0875-59a4-e053-2995a90ab373	2025-12-12	Warnings	Exact identifier application number: M022
Orajel Antiseptic Rinse For All Mouth Sores	HYDROGEN PEROXIDE AND MENTHOL	Church & Dwight Co., Inc.	06188d36-0d60-6ae6-e054-00144ff8d46c	2025-12-12	Warnings	Exact identifier application number: M022
Orajel 3X Medicated For All Mouth Sores	BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	99b589ac-9833-fb60-e053-2995a90a0935	2025-12-12	Warnings	Exact identifier application number: M022
Orajel 4X Medicated For Toothache and Gum, Cream	BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	999aa7b9-bf9e-9285-e053-2a95a90a345b	2025-12-12	Warnings	Exact identifier application number: M022
Orajel 4X Medicated PM For Toothache and Gum	BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	999cff2b-c23e-5abe-e053-2a95a90a7569	2025-12-12	Warnings	Exact identifier application number: M022
Benzoin Compound Tincture	BENZOIN RESIN	Humco Holding Group, Inc.	a893a232-2ea8-4e0d-8cbf-7f5040b3be2e	2025-12-11	Warnings	Exact identifier application number: M022
Listerine Original Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Kenvue Brands LLC	456d45e8-bf6d-31c4-e063-6394a90a5c00	2025-12-10	Warnings	Exact identifier application number: M022
Oral pain relief	BENZOCAINE	ALAINA HEALTHCARE PRIVATE LIMITED	d98c1b2f-fe75-4d52-b082-1abb7628c59e	2025-12-09	Warnings	Exact identifier application number: M022
HEB Sensitive Extra Whitening Twin	SODIUM FLUORIDE	HEB	41d5ae3e-51c1-263b-e063-6394a90a3312	2025-12-08	Warnings	Exact identifier application number: M022
CankerMelts	BENZOCAINE	Quest Products, LLC	070dae82-14c2-66d2-e063-6394a90ab259	2025-12-04	Warnings	Exact identifier application number: M022
Sore Throat ReadyInCase	PHENOL	P & L Development, LLC	2fb3d17e-8ca3-4edb-8b82-4b484f42616e	2025-12-03	Warnings	Exact identifier application number: M022
Listerine Cool Mint Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Kenvue Brands LLC	44f2b66a-26ae-1044-e063-6394a90a9ab6	2025-12-02	Warnings	Exact identifier application number: M022
Sensodyne Fresh Clean	STANNOUS FLUORIDE	Haleon US Holdings LLC	2d433ac1-3ddf-a2f4-e063-6394a90a91f8	2025-12-01	Warnings	Exact identifier application number: M022
Walgreens Saline	NASAL	WALGREEN COMPANY	147e45c8-1e71-4c06-89f1-42e9f9683366	2025-12-01	Warnings	Exact identifier application number: M022
EELHOE Probiotic Bright White Fresh	GLYCERIN	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	425cec0e-aa74-5341-e063-6294a90ac86b	2025-11-27	Warnings	Exact identifier application number: M022
EELHOE 5 Days Tooth Powder	GLYCERIN	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	42f98b14-d1d5-4af8-e063-6294a90a8f67	2025-11-27	Warnings	Exact identifier application number: M022
JAYSUING Colour Corrector	GLYCERIN	Shantou Jaysuing Cleaning and Environmental Protection Technology Co., Ltd.	425d9c23-a692-3c62-e063-6294a90a9404	2025-11-27	Warnings	Exact identifier application number: M022

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
1038929	potassium nitrate 5 % / sodium fluoride 0.24 % Toothpaste	PSN	1e5e8b24-8304-482c-ae80-73effcc345da	4
1038929	potassium nitrate 0.05 MG/MG / sodium fluoride 0.0024 MG/MG Toothpaste	SCD	1e5e8b24-8304-482c-ae80-73effcc345da	4
1038929	K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG Toothpaste	SY	1e5e8b24-8304-482c-ae80-73effcc345da	4
1038929	Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG Toothpaste	SY	1e5e8b24-8304-482c-ae80-73effcc345da	4
1038929	potassium nitrate 5 % / sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste	SY	1e5e8b24-8304-482c-ae80-73effcc345da	4
1038929	potassium nitrate 5 % / sodium fluoride 0.24 % (fluoride ion 0.15 % ) Toothpaste	SY	1e5e8b24-8304-482c-ae80-73effcc345da	4
1038929	potassium nitrate 5 % / sodium fluoride 0.24 % Toothpaste	SY	1e5e8b24-8304-482c-ae80-73effcc345da	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
79481-0009-1	79481000901	1 TUBE in 1 BOX (79481-0009-1) / 113 g in 1 TUBE	1 tube	2020-12-24	0000-00-00	No	No	Current