Crest

Product NDC: 69423-787
11-digit product format: 694230787
Labeler code: 69423
Product ID: 69423-787_47e3a0bc-a062-fbba-e063-6294a90af942
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: 2022-06-15
Substance: SODIUM FLUORIDE
Active strength: 1.6 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	69423-787	69423-787-13	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 · 1 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	69423-787	69423-787-13	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`

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: 3D White Brilliance Luminous Purple
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM FLUORIDE	1.6 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
fbfcd837-4d88-5f82-e053-6394a90afbf6	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
69423-787-13	Crest3D White Brilliance Luminous Purple	130 g in 1 TUBE	PASTE, DENTIFRICE	130	8
69423-787-13	Crest3D White Brilliance Luminous Purple	2 in 1 CARTON	PASTE, DENTIFRICE	2	8
69423-787-34	Crest3D White Brilliance Luminous Purple	130 g in 1 TUBE	PASTE, DENTIFRICE	130	8
69423-787-34	Crest3D White Brilliance Luminous Purple	3 in 1 CARTON	PASTE, DENTIFRICE	3	8
69423-787-35	Crest3D White Brilliance Luminous Purple	1 in 1 CARTON	PASTE, DENTIFRICE	1	8
69423-787-35	Crest3D White Brilliance Luminous Purple	99 g in 1 TUBE	PASTE, DENTIFRICE	99	8
69423-787-46	Crest3D White Brilliance Luminous Purple	1 in 1 CARTON	PASTE, DENTIFRICE	1	8
69423-787-46	Crest3D White Brilliance Luminous Purple	131 g in 1 TUBE	PASTE, DENTIFRICE	131	8
69423-787-85	Crest3D White Brilliance Luminous Purple	24 g in 1 TUBE	PASTE, DENTIFRICE	24	8
69423-787-85	Crest3D White Brilliance Luminous Purple	1 in 1 CARTON	PASTE, DENTIFRICE	1	8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69423-787	CREST 3D WHITE BRILLIANCE LUMINOUS PURPLE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	5	Current NDC, 10 package rows	20250227_fbfcd837-4d88-5f82-e053-6394a90afbf6.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 15 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Anticavity Fluoride Rinse	SODIUM FLUORIDE	Family Dollar Stores, Inc	32ebc633-5338-4d5a-b075-f10b24761248	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity Rinse	SODIUM FLUORIDE	H E B	51ddc81b-1c90-4998-b538-6761ac113437	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	Meijer, Inc.	9a0b6301-2443-41f7-adeb-87578a65c26d	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	CVS Pharmacy, Inc.	344c9d00-ad82-46a9-83e9-68197e1a68bb	2026-02-23	Warnings, Adverse reactions	Exact identifier application number: M021
TheraBreath Complete Oral Rinse	ANTICAVITY ORAL RINSE	Church & Dwight Co., Inc.	27c33ae1-52c7-baad-e063-6394a90a0611	2026-02-23	Warnings	Exact identifier application number: M021
Anticavity Rinse	SODIUM FLUORIDE	Meijer, Inc.	001777fb-196c-499a-94c8-6cdcef0958e9	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	Meijer, Inc.	c628d02f-c834-42b3-b38d-6b9cdcdd0961	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity Rinse	SODIUM FLUORIDE	Meijer, Inc.	b17f7a5d-272e-446d-803b-46a6d8e5f18f	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity Fluoride Rinse	SODIUM FLUORIDE	Meijer, Inc.	d85ce60c-ebff-461f-827a-10fddb9c2bf3	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M021
White Glo Charcoal Baking Soda Maximum White Fluoride Anticavity	SODIUM MONOFLUOROPHOSPHATE	White Glo USA Inc	580c4622-6f9c-48ea-b01e-6ffba7273f24	2026-02-19	Warnings	Exact identifier application number: M021
White Glo Coffee and Tea Stain Remover Fluoride Anticavity	SODIUM MONOFLUOROPHOSPHATE	White Glo USA Inc	f044e213-2403-4f42-a41d-72d58fefcfcb	2026-02-19	Warnings	Exact identifier application number: M021
White Glo Mouthwash Protect Fluoride Anticavity	SODIUM MONOFLUOROPHOSPHATE	White Glo USA Inc	4691584f-8c0c-4589-8b40-89b1779a438d	2026-02-19	Warnings	Exact identifier application number: M021
White Glo Professional Choice Fluoride Anticavity	SODIUM MONOFLUOROPHOSPHATE	White Glo USA Inc	ed8d7506-0385-4422-be77-bcc2db79882f	2026-02-19	Warnings	Exact identifier application number: M021
Alcohol-Free Anticavity	SODIUM FLUORIDE	Meijer, Inc.	c4dcb1d8-f2af-4363-8fcd-c7d1197d66ea	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M021
Oral Antivavity	SODIUM FLUORIDE	Meijer, Inc.	af34f83f-1328-4897-9d04-72ca5a4101bf	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	Meijer, Inc.	acff939e-e98c-4d89-a0c4-0254dc74e672	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity fluoride rinse	SODIUM FLUORIDE	Meijer, Inc.	0bb9fb5f-1893-4187-b60b-05319a8fac6a	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M021
Listerine Total Care Intense Anticavity Fluoride Mouthwash	SODIUM FLUORIDE	Kenvue Brands LLC	4b0404af-309f-7c31-e063-6294a90a5aa1	2026-02-18	Warnings	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	Target Corporation	abfc1973-60ab-44e5-8147-33739d8bd7a3	2026-02-18	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity Fluoride Rinse	SODIUM FLUORIDE	Target Corporation	3e4119b2-9506-4305-8cff-163f700265d0	2026-02-18	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	fbfcd837-4d88-5f82-e053-6394a90afbf6	8
891775	sodium fluoride 0.00243 MG/MG Toothpaste	SCD	fbfcd837-4d88-5f82-e053-6394a90afbf6	8
891775	sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste	SY	fbfcd837-4d88-5f82-e053-6394a90afbf6	8
891775	sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste	SY	fbfcd837-4d88-5f82-e053-6394a90afbf6	8
891775	sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste	SY	fbfcd837-4d88-5f82-e053-6394a90afbf6	8
891775	sodium fluoride 0.243 % (fluoride ion 0.16 % ) Toothpaste	SY	fbfcd837-4d88-5f82-e053-6394a90afbf6	8

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
69423-787-13	69423078713	130 g in 1 TUBE	130 g				Historical
69423-787-34	69423078734	3 TUBE in 1 CARTON (69423-787-34) / 130 g in 1 TUBE	3 tube	2022-06-15	No	No	Current
69423-787-35	69423078735	1 TUBE in 1 CARTON (69423-787-35) / 99 g in 1 TUBE	1 tube	2022-06-15	No	No	Current
69423-787-46	69423078746	1 TUBE in 1 CARTON (69423-787-46) / 131 g in 1 TUBE	1 tube	2022-06-15	No	No	Current
69423-787-85	69423078785	1 TUBE in 1 CARTON (69423-787-85) / 24 g in 1 TUBE	1 tube	2022-06-15	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Crest 3D White Brilliance Luminous Purple	The Procter & Gamble Manufacturing Company	2026-01-08	HUMAN OTC DRUG LABEL	8