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 28 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Crest Pro-Health Gum Detoxify Plus	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	2f9e346e-d664-81d5-e063-6394a90a4525	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Holiday Smile Deep Stain Remover and Whitestrips	SODIUM MONOFLUOROPHOSPHATE	The Procter & Gamble Manufacturing Company	3c57d487-a3c7-b238-e063-6294a90aed81	2026-01-08		Exact identifier application number: M021
Crest Complete plus Scope Pro Advanced Freshness	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	325c3ab2-aaa2-a06f-e063-6294a90abefb	2026-01-08	Warnings	Exact identifier application number: M021
Crest Tartar Protection	SODIUM FLUORIDE	Procter & Gamble Manufactura, S. de R.L. de C.V.	5940711d-71b7-cb7d-e053-2a91aa0aef18	2026-01-08	Warnings	Exact identifier application number: M021
Meijer Restore and Defend Sensitive	STANNOUS FLUORIDE	Meijer Distribution Inc	82bdfdb5-39f2-8c09-e053-2991aa0a096c	2026-01-08	Warnings	Exact identifier application number: M021
Crest Strawberry	SODIUM FLUORIDE	Procter & Gamble Manufactura, S. de R.L. de C.V.	01f69824-e886-6e7b-e063-6294a90acf77	2026-01-08	Warnings	Exact identifier application number: M021
Crest Bubblegum	SODIUM FLUORIDE	Procter & Gamble Manufacturing Mxico, S. de R.L. de C.V.	01f64874-6363-3dcc-e063-6394a90a2aec	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Fresh Mint	SODIUM FLUORIDE	Procter & Gamble Manufactura, S. de R.L. de C.V.	01f27a63-15f3-cee4-e063-6394a90afa3b	2026-01-08	Warnings	Exact identifier application number: M021
Crest Bubblegum	SODIUM FLUORIDE	Procter & Gamble Manufacturing Mxico, S. de R.L. de C.V.	01f618d7-be07-18c3-e063-6294a90a2d97	2026-01-08	Warnings	Exact identifier application number: M021
Crest Strawberry	SODIUM FLUORIDE	Procter & Gamble Manufactura, S. de R.L. de C.V.	01f35279-76ce-6027-e063-6294a90a8e34	2026-01-08	Warnings	Exact identifier application number: M021
Crest Snowberry	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	42ca1f06-3e7d-8fed-e063-6394a90afbff	2026-01-08	Warnings	Exact identifier application number: M021
Crest Strawberry	SODIUM FLUORIDE	Procter & Gamble Manufactura, S. de R.L. de C.V.	7d615c52-f9c9-4856-e053-2991aa0a7927	2026-01-08	Warnings	Exact identifier application number: M021
Crest Fresh and White	SODIUM FLUORIDE	Procter & Gamble Manufactura, S. de R.L. de C.V.	5a1bb1fb-12a5-5fd1-e053-2991aa0a628b	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Stain Eraser Icy Clean Mint	SODIUM FLUORIDE	Procter & Gamble Manufacturing Mxico, S. de R.L. de C.V.	8de12c9f-eb16-aa26-e053-2a95a90a1b9c	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro Health Peppermint Frost	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	42c84772-d406-b6ca-e063-6394a90a920f	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Sparkle Mint	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	42cb1b2a-55ad-cb9c-e063-6294a90ac88c	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro-Health Gum Recession	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	47be4eff-1ab5-17a1-e063-6394a90ae465	2026-01-08	Warnings	Exact identifier application number: M021
Supersmile Professional Whitening TP	SODIUM MONOFLUOROPHOSPHATE	Robell Research, Inc	25021787-44e8-0b29-e063-6394a90a0af6	2026-01-08	Warnings	Exact identifier application number: M021
Supersmile Professional whitening TP Original Mint	SODIUM MONOFLUOROPHOSPHATE	Robell Research, Inc	2502c305-71ab-bb71-e063-6394a90a0a84	2026-01-08	Warnings	Exact identifier application number: M021
Supersmile Professional Whitening TP Original Mint	SODIUM MONOFLUOROPHOSPHATE	Robell Research, Inc	2502840c-82ee-12cb-e063-6394a90a5b3f	2026-01-08	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

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