AIM

Product NDC: 10237-630
11-digit product format: 102370630
Labeler code: 10237
Product ID: 10237-630_5593d974-6d63-d952-e063-6394a90af155
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Fluoride
Dosage form: GEL, DENTIFRICE
Route: DENTAL
Labeler: Church & Dwight Co., Inc.
Application: M021
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2010-11-10
Substance: SODIUM FLUORIDE
Active strength: 2.4 mg/g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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	10237-630	10237-630-60	D	Discontinued by firm		2026-10-12

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 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	10237-630-60	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	10237-630-60	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	10237-630-60	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	10237-630-60	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	10237-630-60	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	10237-630-60	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	10237-630-60	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	10237-630-60	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	10237-630-60	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	10237-630-60	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	10237-630-60	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	10237-630-60	`557ba5c1ecfa…`	`9c80585c8c6e…`

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: AIM
Brand name suffix: Cavity Protection with Whitening
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM FLUORIDE	2.4 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
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
416783	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
a8c742e1-ee61-4593-b8f5-b9e586d39dfc	Available on FDA.report

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
CARBOXYMETHYLCELLULOSE SODIUM	INACTIVE INGREDIENT	K679OBS311	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
D&C RED NO. 33	INACTIVE INGREDIENT	9DBA0SBB0L	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
HYDRATED SILICA	INACTIVE INGREDIENT	Y6O7T4G8P9	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
MICA	INACTIVE INGREDIENT	V8A1AW0880	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
PEG-32 STEARATE	INACTIVE INGREDIENT	33GX5WQC0M	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
SORBITOL	INACTIVE INGREDIENT	506T60A25R	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	AIM CAVITY PROTECTION WITH WHITENING (SODIUM FLUORIDE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	2

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 29 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Supersmile Professional Whitening TP Citrus Blast	SODIUM MONOFLUOROPHOSPHATE	Robell Research, Inc	25039552-c35d-a69d-e063-6394a90ab103	2026-01-08	Warnings	Exact identifier application number: M021
Supersmile Professional Whitening TP Citrus Blast	SODIUM MONOFLUOROPHOSPHATE	Robell Research, Inc	2504686d-b053-51d0-e063-6394a90a789f	2026-01-08	Warnings	Exact identifier application number: M021
Supersmile Professional Whitening TP Peppy Mint 8 oz	SODIUM MONOFLUOROPHOSPHATE	Robell Research, Inc	25121ebb-922b-719d-e063-6394a90a23d3	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro-health Gum Detoxify Deep Clean	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	f498b727-c38c-1d67-e053-2995a90a0f11	2026-01-08	Warnings	Exact identifier application number: M021
DG health Sensitive Maximum Strength	POTASSIUM NITRATE, SODIUM FLUORIDE	Dolgencorp, LLC	81cd5d37-3751-625f-e053-2a91aa0a6dfd	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Glamorous White	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	f5b18988-68c7-40f9-e053-2995a90a22bc	2026-01-08	Warnings	Exact identifier application number: M021
CVS Restore and Defend Sensitive Whitening	STANNOUS FLUORIDE	CVS Pharmacy	81b72da2-7f41-74ca-e053-2a91aa0a9646	2026-01-08	Warnings	Exact identifier application number: M021
Gum and Enamel Repair	STANNOUS FLUORIDE	CVS	ccad05d4-7f05-bebd-e053-2a95a90aa52c	2026-01-08	Warnings	Exact identifier application number: M021
CVS Pharmacy Pro Defense	FLUORIDE	CVS Pharmacy	445ec57e-dc3c-49a0-8ca9-4806fcdc0303	2026-01-08	Warnings	Exact identifier application number: M021
Gum Detoxify	STANNOUS FLUORIDE	Walmart	ad3f645d-aaf9-2800-e053-2a95a90ab62f	2026-01-08	Warnings	Exact identifier application number: M021
CVS Complete Protection	STANNOUS FLOURIDE	CVS	b681b5e4-a0e1-8d0f-e053-2a95a90aa672	2026-01-06	Warnings	Exact identifier application number: M021
Complete Protection	STANNOUS FLUORIDE	Target	03708e08-0189-b83d-e063-6394a90a50e6	2026-01-06	Warnings	Exact identifier application number: M021
Brush Buddies Mouthwash 12oz Star Wars Saber Strike Strawberry	SODIUM FLUORIDE	Kingkey MBC Life Technology Group co., LTD.	4998c0e6-1de3-11cd-e063-6294a90acb6f	2026-01-01	Warnings	Exact identifier application number: M021
Exceed Total Care Sensitive Spearmint Tooth Polish	POTASSIUM NITRATE AND SODIUM FLUORIDE	Melaleuca, Inc	dc620d3f-880f-df05-e053-2995a90a8409	2025-12-31	Warnings	Exact identifier application number: M021
Exceed Total Care Sensitive Peppermint Tooth Polish	POTASSIUM NITRATE AND SODIUM FLUORIDE	Melaleuca, Inc	ed2179a4-3d19-6481-e053-2995a90ad655	2025-12-31	Warnings	Exact identifier application number: M021
Koala Pals Berrylicious	SODIUM FLUORIDE	Melaleuca, Inc.	6624be86-c9a8-53b8-e053-2a91aa0a87ef	2025-12-31	Warnings	Exact identifier application number: M021
Whitening Tooth Polish	SODIUM FLUORIDE	Melaleuca, Inc.	6893405a-a2c4-068e-e053-2a91aa0ae5b1	2025-12-31	Warnings	Exact identifier application number: M021
Gel 1100 Mint	SODIUM FLUORIDE	Dental Alliance Holdings LLC	f125fb04-5045-5367-e053-2a95a90aa73b	2025-12-29	Warnings	Exact identifier application number: M021
Gracie Square Hospital Amenity	SODIUM MONOFLUOROPHOSPHATE	ASP Global, LLc	89d81053-6950-465e-a5b1-cbf841d7afcb	2025-12-29	Warnings	Exact identifier application number: M021
CloSYS Fluoride Rinse	SODIUM FLUORIDE	Rowpar Pharmaceuticals, Inc.	1a994f24-99ee-4b27-aab0-e816931a22c8	2025-12-23	Warnings	Exact identifier application number: M021

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
8ZYQ1474W7	SODIUM FLUORIDE	7681-49-4	SODIUM FLUORIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
10237-630-45	10237063045	1 TUBE in 1 CARTON (10237-630-45) / 127 g in 1 TUBE	1 tube	2026-07-01	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
AIM Multi-Benefit Cavity Protection with Whitening CinnaMint Gel	Church & Dwight Co., Inc.	2026-07-01	HUMAN OTC DRUG LABEL	4

AIM