Murchison Hume Dental Kit

Product NDC: 69491-034
11-digit product format: 694910034
Labeler code: 69491
Product ID: 69491-034_0cfd6fe3-2662-be85-e063-6394a90a5e04
Type: HUMAN OTC DRUG
Nonproprietary name: SODIUM MONOFLUOROPHOSPHATE
Dosage form: KIT
Labeler: Buzz Products Inc.
Application: M021
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-10-15
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 · 22 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	69491-034-01	`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	69491-034-01	`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	69491-034-01	`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	69491-034-01	`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	69491-034-01	`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	69491-034-01	`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	69491-034-01	`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	69491-034-01	`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	69491-034-01	`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	69491-034-01	`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	69491-034-01	`367a005e9d99…`	`383a685ebd0f…`

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: Murchison Hume Dental Kit
Listing expiration: 2026-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
545626	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
b1a442e1-86cf-cba6-e053-2995a90a593a	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69491-034-01	2025-12-16	C162847	48780-1	1030e365-13ab-111a-e063-dadaa90a10e2	Murchison-Hume Dental Kit Toothbrush and Toothpaste
69491-034-01	2024-07-30	C162847	48780-1	1030e365-13ab-111a-e063-dadaa90a10e2	Murchison-Hume Dental Kit Toothbrush and Toothpaste
69491-034-01	2024-01-30	C162847	48780-1	1030e365-13ab-111a-e063-dadaa90a10e2	Murchison-Hume Dental Kit Toothbrush and Toothpaste

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69491-034-01	Murchison Hume Dental Kit	1 in 1 KIT	KIT	1		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69491-034	MURCHISON HUME DENTAL KIT (SODIUM MONOFLUOROPHOSPHATE) KIT [BUZZ EXPORT SERVICES PTY., LTD.]	3	Current NDC, Legacy NDC, 1 package rows	20230111_b1a442e1-86cf-cba6-e053-2995a90a593a.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 51 · 1,013 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
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
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

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
C810JCZ56Q	SODIUM MONOFLUOROPHOSPHATE	10163-15-2	SODIUM MONOFLUOROPHOSPHATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
545626	sodium monofluorophosphate 0.76 % Toothpaste	PSN	b1a442e1-86cf-cba6-e053-2995a90a593a	4
545626	sodium monofluorophosphate 0.0076 MG/MG Toothpaste	SCD	b1a442e1-86cf-cba6-e053-2995a90a593a	4
545626	sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste	SY	b1a442e1-86cf-cba6-e053-2995a90a593a	4
545626	sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste	SY	b1a442e1-86cf-cba6-e053-2995a90a593a	4
545626	sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )Toothpaste	SY	b1a442e1-86cf-cba6-e053-2995a90a593a	4
545626	sodium monofluorophosphate 0.76 % (fluoride ion 0.15 % )Toothpaste	SY	b1a442e1-86cf-cba6-e053-2995a90a593a	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69491-034-01	69491003401	1 KIT in 1 KIT (69491-034-01) * 10 g in 1 TUBE (69491-033-01)	1 kit	2020-10-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Murchison-Hume Dental Kit Toothbrush and Toothpaste	Buzz Products Inc.	2023-12-20	HUMAN OTC DRUG LABEL	4