Crest

Product NDC: 69423-897
11-digit product format: 694230897
Labeler code: 69423
Product ID: 69423-897_47e4bcee-5026-eff8-e063-6294a90a9a3c
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Fluoride
Dosage form: PASTE, DENTIFRICE
Route: DENTAL
Labeler: The Procter & Gamble Manufacturing Company
Application: M021
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-10-01
Substance: SODIUM FLUORIDE
Active strength: 1.5 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 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded package	package	69423-897	69423-897-29	D	Discontinued by firm	2026-10-12
excluded package	package	69423-897	69423-897-57	D	Discontinued by firm	2026-10-12
excluded package	package	69423-897	69423-897-64	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 · 6 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	69423-897-57	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	69423-897-64	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	69423-897-29	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	69423-897-57	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	69423-897-64	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	69423-897-29	`f5e01cc5f278…`	`a2eaf40c39c3…`

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: Crest
Brand name suffix: Fresh and White
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM FLUORIDE	1.5 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
891775	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
f9b31f6b-6b3f-abe0-e053-6294a90acb25	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
69423-897-24	CrestFresh and White	68 g in 1 TUBE	PASTE, DENTIFRICE	68	5
69423-897-24	CrestFresh and White	1 in 1 CARTON	PASTE, DENTIFRICE	1	5
69423-897-29	CrestFresh and White	1 in 1 CARTON	PASTE, DENTIFRICE	1	5
69423-897-29	CrestFresh and White	82 g in 1 TUBE	PASTE, DENTIFRICE	82	5
69423-897-57	CrestFresh and White	1 in 1 CARTON	PASTE, DENTIFRICE	1	5
69423-897-57	CrestFresh and White	161 g in 1 TUBE	PASTE, DENTIFRICE	161	5
69423-897-64	CrestFresh and White	1 in 1 CARTON	PASTE, DENTIFRICE	1	5
69423-897-64	CrestFresh and White	181 g in 1 TUBE	PASTE, DENTIFRICE	181	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69423-897	CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3	Current NDC, 8 package rows	20250110_f9b31f6b-6b3f-abe0-e053-6294a90acb25.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 14 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Anticavity	SODIUM FLUORIDE	Old East Main Co.	64f3d92d-f58c-4bc2-8819-f91492221ddb	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	Old East Main Co.	c7b9e9cd-3cf7-4657-83c9-e221e1c35977	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M021
Instant Whitening	INSTANT WHITENING TOOTHPASTE	Guangzhou City Caiye Cosmetics CO., Ltd	2807ece8-a1a5-b626-e063-6394a90aac62	2026-03-02	Warnings	Exact identifier application number: M021
Coffe Tea Stain Remover Tooth	COFFE TEA STAIN REMOVER TOOTHPASTE	Guangzhou City Caiye Cosmetics CO., Ltd	2845d7af-7a0b-9bc8-e063-6294a90ac8b3	2026-03-02	Warnings	Exact identifier application number: M021
Professional whitening tooth	PROFESSIONAL WHITENING TOOTHPASTE	Guangzhou City Caiye Cosmetics CO., Ltd	291eba71-14da-fac3-e063-6294a90aa3cc	2026-03-02	Warnings	Exact identifier application number: M021
purple tooth	PURPLE TOOTHPASTE	Guangzhou City Caiye Cosmetics CO., Ltd	291f0312-238c-71d5-e063-6294a90a39e1	2026-03-02	Warnings	Exact identifier application number: M021
Professional Choice	PROFESSIONAL CHOICE TOOTHPASTE	Guangzhou City Caiye Cosmetics CO., Ltd	28406739-6a8c-1ce8-e063-6394a90a08f8	2026-03-02	Warnings	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	The Kroger Co.	27a98b64-8369-4f3d-b487-d7ce98abc69f	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	The Kroger Co.	390dd1b5-2dd1-4b55-b4b3-e441ada61238	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Alcohol-Free Anticavity	SODIUM FLUORIDE	The Kroger Co.	5459eeee-adf0-4afe-b190-62d4fa113806	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Oral Antivavity	SODIUM FLUORIDE	The Kroger Co.	932723b8-9875-4f37-8c11-018c94ae0ae1	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	The Kroger Co.	d0c552d8-44ad-4d95-b3fb-17015f44b334	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity Rinse	SODIUM FLUORIDE	Walmart Inc.	3beb65e4-ae8e-4e51-b9ba-181cbec41eff	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	Walmart Inc.	61669087-0af6-4192-b514-afcfe7d8ba98	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	Walmart Inc.	e79e43e6-d6b6-4df4-9d9f-fe9fe35f180d	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Alcohol-Free Anticavity	SODIUM FLUORIDE	Walmart Inc.	1fd2f3ca-066e-282a-e063-6294a90a05a9	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	Walmart Inc.	af5b93e7-5cce-4e01-8df2-54494d8b2910	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	Walmart Inc.	4590ca97-130c-46b2-9ba0-38f4703ef30a	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M021
Colgate Anticavity	SODIUM MONOFLUOROPHOSPHATE	MING FAI ENTERPRISE (CAMBODIA) CO., LTD.	4ba81636-cdb7-e904-e063-6394a90a8bd5	2026-02-25	Warnings	Exact identifier application number: M021
Anticavity Rinse	SODIUM FLUORIDE	Family Dollar Stores, Inc	32a92add-c9db-4733-8e35-613825fdf081	2026-02-24	Warnings, Adverse reactions	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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
891775	sodium fluoride 0.243 % Toothpaste	PSN	f9b31f6b-6b3f-abe0-e053-6294a90acb25	5
891775	sodium fluoride 0.00243 MG/MG Toothpaste	SCD	f9b31f6b-6b3f-abe0-e053-6294a90acb25	5
891775	sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste	SY	f9b31f6b-6b3f-abe0-e053-6294a90acb25	5
891775	sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste	SY	f9b31f6b-6b3f-abe0-e053-6294a90acb25	5
891775	sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste	SY	f9b31f6b-6b3f-abe0-e053-6294a90acb25	5
891775	sodium fluoride 0.243 % (fluoride ion 0.16 % ) Toothpaste	SY	f9b31f6b-6b3f-abe0-e053-6294a90acb25	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
69423-897-24	69423089724	1 TUBE in 1 CARTON (69423-897-24) / 68 g in 1 TUBE	1 tube	2021-10-01	No	No	Current
69423-897-29	69423089729	1 in 1 CARTON					Historical
69423-897-57	69423089757	1 in 1 CARTON					Historical
69423-897-64	69423089764	1 in 1 CARTON					Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Crest Fresh and White Peppermint Gleem Toothpaste	The Procter & Gamble Manufacturing Company	2026-01-08	HUMAN OTC DRUG LABEL	5