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 34 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hello Whipped Mellow Mint Dream Flavor	SODIUM MONOFLUOROPHOSPHATE	Colgate-Palmolive Company	7a72b687-475d-437a-9734-a29637e5516a	2025-11-11	Warnings	Exact identifier application number: M021
Spry Dentifrice	TOOTHPASTE	Xlear Inc.	43567bbc-b07e-b605-e063-6294a90aad78	2025-11-11	Warnings	Exact identifier application number: M021
Hello Naturally Whitening	SODIUM MONOFLUOROPHOSPHATE	COLGATE PALMOLIVE COMPANY	5ad241e1-6bfc-7863-6a7a-100753651f0a	2025-11-11	Warnings	Exact identifier application number: M021
Hello Whipped Peppermint Stick Flavor	SODIUM MONOFLUOROPHOSPHATE	Colgate-Palmolive Company	d6c4ac9e-f55e-4ebc-bd6a-e39eaeb4f813	2025-11-11	Warnings	Exact identifier application number: M021
Super Mint	MINT TOOTHPASTE	SuperMouth, LLC.	d23e89f5-7b65-4ed9-803a-38233f30d8f2	2025-11-07	Warnings	Exact identifier application number: M021
Dentisse	SODIUM FLUORIDE	Dentisse, Inc.	326b290a-9bd2-468e-e054-00144ff8d46c	2025-11-04	Warnings	Exact identifier application number: M021
Home Care Fluoride	STANNOUS FLUORIDE	Dental Technologies, Inc.	51f1d84c-809a-4c96-a117-7a8d8aa1e6b4	2025-11-04	Warnings	Exact identifier application number: M021
Home Care Fluoride	STANNOUS FLUORIDE	Dental Technologies, Inc.	c44686f8-93ee-4a8f-8481-3439d123f6d2	2025-11-04	Warnings	Exact identifier application number: M021
Home Care Fluoride	STANNOUS FLUORIDE	Dental Technologies, Inc.	16ebcb37-5703-4e10-b965-570e18434b52	2025-11-04	Warnings	Exact identifier application number: M021
Plak Smacker GREAT WHITE SHARK	SODIUM FLUORIDE	YOUNG PS ACQUISITION, LLC	ca5b91aa-f69c-4553-a2b6-acf0ca1d920e	2025-11-04	Warnings	Exact identifier application number: M021
Plak Smacker	STANNOUS FLUORIDE	Young Innovations, Inc.	e65fa41e-ce2e-53e4-e053-2995a90a24d2	2025-11-04	Warnings	Exact identifier application number: M021
Plak Smacker	STANNOUS FLUORIDE	Young Innovations, Inc.	e65c62d9-e8a6-3101-e053-2995a90a1494	2025-11-04	Warnings	Exact identifier application number: M021
Home Care Fluoride	STANNOUS FLUORIDE	Dental Technologies, Inc.	15bdc03e-2cc7-4b7d-96fc-4f3236ed5c75	2025-11-04	Warnings	Exact identifier application number: M021
Strawberry Flavor Sodium Fluoride Anticavity Toothpast	SODIUM FLUORIDE	HISMILE PTY LTD	426c2aca-ca2b-5e34-e063-6294a90ae37c	2025-11-02	Warnings	Exact identifier application number: M021
Watermelon Flavor Sodium Fluoride Anticavity Toothpast	SODIUM FLUORIDE	HISMILE PTY LTD	426e40cb-e30d-0db1-e063-6294a90a762b	2025-10-31	Warnings	Exact identifier application number: M021
Classic Mint Flavor Sodium Fluoride Anticavity Toothpast	SODIUM FLUORIDE	HISMILE PTY LTD	425a9b71-5a7f-83e6-e063-6394a90ab703	2025-10-30	Warnings	Exact identifier application number: M021
Grape Bubblegum Flavor Sodium Fluoride Anticavity Toothpast	SODIUM FLUORIDE	HISMILE PTY LTD	425b1a2e-7576-13a7-e063-6394a90aa865	2025-10-30	Warnings	Exact identifier application number: M021
The Simpsons Pink Donut Flavor Sodium Fluoride Anticavity Toothpast	SODIUM FLUORIDE	HISMILE PTY LTD	426b8efa-e691-a67d-e063-6394a90abf8d	2025-10-30	Warnings	Exact identifier application number: M021
Blue Raspberry Flavor Sodium Fluoride Anticavity Toothpast	SODIUM FLUORIDE	HISMILE PTY LTD	42583b32-525f-925d-e063-6294a90af76f	2025-10-29	Warnings	Exact identifier application number: M021
PERIOE KAKAO KIDS Strawberry	SODIUM FLUORIDE	LG HOUSEHOLD & HEALTH CARE LTD.	4239f8c2-a5f5-3fa6-e063-6294a90acb47	2025-10-28	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