Quip

Product NDC: 69261-002
11-digit product format: 692610002
Labeler code: 69261
Product ID: 69261-002_2cf3292d-d1b4-81ea-e063-6294a90a215e
Type: HUMAN OTC DRUG
Nonproprietary name: SODIUM FLUORIDE
Dosage form: PASTE, DENTIFRICE
Route: DENTAL
Labeler: Quip NYC Inc.
Application: M021
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-07-18
Substance: SODIUM FLUORIDE
Active strength: .23 g/100g
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 · 27 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
2025-02-02 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	69261-002-01	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	69261-002-02	`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	69261-002-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	69261-002-02	`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	69261-002-01	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	69261-002-02	`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	69261-002-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	69261-002-02	`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	69261-002-01	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	69261-002-02	`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	69261-002-01	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	69261-002-02	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	69261-002-01	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	69261-002-02	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	69261-002-01	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	69261-002-02	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	69261-002-01	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	69261-002-02	`1332a3947898…`	`d4bfe170f9cd…`

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: Quip
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM FLUORIDE	.23 g/100g

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
1489127	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
714b7205-444d-929b-e053-2995a90a958e	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5eb9f24b-9328-475e-af0a-18021935eb6a	Product name	1	20180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
69261-002-01	2025-02-01	Quip Anticavity Toothpaste
69261-002-02	2025-02-01	Quip Anticavity Toothpaste
69261-002-01	2023-01-30	Quip Anticavity Toothpaste
69261-002-02	2023-01-30	Quip Anticavity Toothpaste

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
69261-002-01	Quip	133 g in 1 TUBE	PASTE, DENTIFRICE	133	3
69261-002-01	Quip	1 in 1 CARTON	PASTE, DENTIFRICE	1	3
69261-002-02	Quip	24 g in 1 TUBE	PASTE, DENTIFRICE	24	3
69261-002-02	Quip	1 in 1 CARTON	PASTE, DENTIFRICE	1	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69261-002	QUIP (SODIUM FLUORIDE) PASTE, DENTIFRICE [QUIP NYC INC.]	3	Current NDC, Legacy NDC, 4 package rows	20250201_714b7205-444d-929b-e053-2995a90a958e.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
1489127	sodium fluoride 0.23 % Toothpaste	PSN	714b7205-444d-929b-e053-2995a90a958e	3
1489127	sodium fluoride 0.0023 MG/MG Toothpaste	SCD	714b7205-444d-929b-e053-2995a90a958e	3
1489127	sodium fluoride 0.23 % Toothpaste	SY	714b7205-444d-929b-e053-2995a90a958e	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69261-002-01	69261000201	1 TUBE in 1 CARTON (69261-002-01) / 133 g in 1 TUBE	1 tube	2018-07-18	0000-00-00	No	No	Current
69261-002-02	69261000202	1 TUBE in 1 CARTON (69261-002-02) / 24 g in 1 TUBE	1 tube	2018-07-18	0000-00-00	No	No	Current