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 32 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Colgate Anticavity Kit	SODIUM MONOFLUOROPHOSPHATE	Ming Fai Industrial (Shenzhen) Co. Ltd	86dfd09d-f3b6-4c4b-852d-7e04dc5c8fec	2025-12-05	Warnings	Exact identifier application number: M021
Dr. Jen SuperPaste Nano-Hydroxyapatite	SODIUM FLUORIDE	Dr Jen Natural, LLC	8b28b857-9162-4065-b0a0-571efffe9787	2025-12-05	Warnings	Exact identifier application number: M021
Dr. Jen SuperPaste Ortho	SODIUM FLUORIDE	Dr Jen Natural, LLC	9dd248bf-9488-43cd-a041-e8315a05ce5d	2025-12-04	Warnings	Exact identifier application number: M021
Dr. Jen SuperPaste Perio	SODIUM FLUORIDE	Dr Jen Natural, LLC	8c7e6d3a-49d9-4098-9d5e-e9792b373574	2025-12-04	Warnings	Exact identifier application number: M021
Colgate Total Plaque Cleanse	STANNOUS FLUORIDE	Colgate-Palmolive Company	b2980238-5bcb-467f-9e90-a307938632c2	2025-12-03	Warnings	Exact identifier application number: M021
Advance White Extreme Whitening Tartar Control	SODIUM FLUORIDE	Church & Dwight Co., Inc.	b539264f-e1ff-440b-af76-84266fe2c0a2	2025-12-02	Warnings	Exact identifier application number: M021
Sensodyne Pronamel Clinical Enamel Strength Fresh Breath	POTASSIUM NITRATE, SODIUM FLUORIDE	Haleon US Holdings LLC	34a1a32e-3017-f018-e063-6394a90a0230	2025-12-01	Warnings	Exact identifier application number: M021
PRO-SYS	SODIUM FLUORIDE AND POTASSIUM NITRATE	Benco Dental	4e470ba4-60bb-1815-e063-6294a90abacc	2025-12-01	Warnings	Exact identifier application number: M021
PRO-SYS	SODIUM FLUORIDE	Benco Dental	4e539cb2-bcbd-95fc-e063-6294a90a2121	2025-12-01	Warnings	Exact identifier application number: M021
Cool sense Care Plus	SODIUM FLUORIDE	DONG IL PHARMS CO., LTD.	44763bf6-caf3-ec69-e063-6394a90a0ee1	2025-11-25	Warnings	Exact identifier application number: M021
DOCTRUST DOUBLEX Tooth	SODIUM FLUORIDE	DONG IL PHARMS CO.,LTD	44765e86-2eb2-6381-e063-6394a90a761f	2025-11-25	Warnings	Exact identifier application number: M021
TheraBreath for Kids Anticavity Wacky Watermelon	SODIUM FLUORIDE	Church & Dwight Co., Inc.	578f8010-6b1c-4c6b-91d3-e483ace40f66	2025-11-25	Warnings	Exact identifier application number: M021
Sensodyne Cavity and Sensitivity	POTASSIUM NITRATE, SODIUM FLUORIDE	Haleon US Holdings LLC	d002074b-0580-4247-b3c7-121b8c098697	2025-11-24	Warnings	Exact identifier application number: M021
CVS Pharmacy Enamel Guard	FLUORIDE	CVS Pharmacy	18295a1c-c2a6-489b-be34-9252b9e1e2b8	2025-11-21	Warnings	Exact identifier application number: M021
365 Everyday Value Cavity Fighting and Whitening	SODIUM MONOFLOUROPHOSPHATE	Whole Foods Market, Inc.	83704717-19bc-2634-e053-2991aa0a2979	2025-11-21	Warnings	Exact identifier application number: M021
Whitening	MONOFLUOROPHOSPHATE	Target	0074630f-9d8d-9209-e063-6294a90a4f01	2025-11-21	Warnings	Exact identifier application number: M021
Rite Aid Enamel Guard	FLUORIDE	Rite Aid	67c1fc04-0f21-4944-8b9d-0d8ffd051874	2025-11-21	Warnings	Exact identifier application number: M021
ME MOTHER EARTH	ZERO WASTE TOOTHPASTE TABLETS PEPPERMINT	A PLUS MERCHANDISE LLC	43d30abc-889a-5377-e063-6294a90ab804	2025-11-17	Warnings	Exact identifier application number: M021
Natural White Sensitivity and Gum	STANNOUS FLUORIDE	Lornamead Products	2e83bda8-4d4b-640f-e063-6294a90abc60	2025-11-14	Warnings	Exact identifier application number: M021
CVS Pharmacy Restore and Defend	FLUORIDE	CVS Pharmacy	99f86135-05b7-42b1-aef5-df4513259b8f	2025-11-14	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