Anticavity Fluoride Rinse

Product NDC: 41163-213
11-digit product format: 411630213
Labeler code: 41163
Product ID: 41163-213_4af77d6f-72cf-9e71-e063-6294a90ab81c
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Fluoride
Dosage form: MOUTHWASH
Route: ORAL
Labeler: United Natural Foods, Inc. dba UNFI
Application: M021
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2009-05-14
Substance: SODIUM FLUORIDE
Active strength: .2 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
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 · 14 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	41163-213-44	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	41163-213-44	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	41163-213-44	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	41163-213-44	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	41163-213-44	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	41163-213-44	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	41163-213-44	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`

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: Anticavity Fluoride Rinse
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM FLUORIDE	.2 mg/mL

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
240698	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
e696038c-182e-4325-9b90-87fe498d9f67	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
41163-213-44	2023-01-20	C162847	48780-1	9d75b9cf-ffb9-f424-e053-dadaa90a57ce	Equaline 213.001/213AE rev 2 Anticavity Fluoride Rinse, Mint
41163-213-44	2020-01-31	C162847	48780-1	9d75b9cf-ffb9-f424-e053-dadaa90a57ce	Equaline 213.001/213AE rev 2 Anticavity Fluoride Rinse, Mint

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41163-213-44	Anticavity Fluoride Rinse	532 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	532		8

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
CETYLPYRIDINIUM CHLORIDE	INACTIVE INGREDIENT	D9OM4SK49P	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
MENTHOL	INACTIVE INGREDIENT	L7T10EIP3A	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
METHYL SALICYLATE	INACTIVE INGREDIENT	LAV5U5022Y	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
POLOXAMER 407	INACTIVE INGREDIENT	TUF2IVW3M2	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
POLYSORBATE 20	INACTIVE INGREDIENT	7T1F30V5YH	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
POTASSIUM SORBATE	INACTIVE INGREDIENT	1VPU26JZZ4	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
SODIUM PHOSPHATE	INACTIVE INGREDIENT	SE337SVY37	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [SUPERVALU, INC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41163-213	ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [UNITED NATURAL FOODS, INC. DBA UNFI]	7	Current NDC, Legacy NDC, 1 package rows	20250410_e696038c-182e-4325-9b90-87fe498d9f67.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 24 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Crest Pro Health Sensitive and Enamel Shield	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	fb48b15c-f821-e5cd-e053-6294a90ac64c	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Brilliance Luminous Purple	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	fbfcd837-4d88-5f82-e053-6394a90afbf6	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro Health with a Touch of Scope	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	fb572b41-36cd-55d7-e053-6394a90a71c8	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro Health Whitening Gel	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	fb5b1e94-bed6-8486-e053-6294a90a3a84	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Ultra Vivid Mint	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	cba96ef0-0519-059f-e053-2a95a90a43ad	2026-01-08	Warnings	Exact identifier application number: M021
Crest 4in1	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	ce545406-3c4f-1ba7-e053-2a95a90a91ac	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Whitening	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	d218ddc0-1d5f-f39b-e053-2995a90a96ed	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro Health Advanced Antibacterial Protection	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	d58bc842-2687-e52d-e053-2995a90a5433	2026-01-08	Warnings	Exact identifier application number: M021
Scope Stay Strong	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	d65b3153-2026-a8c0-e053-2a95a90a31d6	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro Health Advanced Whitening Charcoal	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	d6f68485-b92f-41c7-e053-2995a90a4fe5	2026-01-08	Warnings	Exact identifier application number: M021
KIDS Crest Advanced Enamel Plus Cavity Protection	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	d837ecde-249a-7868-e053-2a95a90a56ae	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro Health Advanced Whitening Intensive Cleaning	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	d6fa4187-a651-647b-e053-2995a90a8567	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro Health Advanced Gum Protection	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	d7729dde-c828-34e6-e053-2a95a90a5ee6	2026-01-08	Warnings	Exact identifier application number: M021
Crest Densify Daily Whitening	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	d811306f-4994-7a5a-e053-2995a90adf16	2026-01-08	Warnings	Exact identifier application number: M021
Crest Densify Daily Protection	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	d810d4e5-ba66-efe1-e053-2995a90abfc0	2026-01-08	Warnings	Exact identifier application number: M021
Crest Braces Care Cavity Protection	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	d823cba4-c4cf-7d7a-e053-2995a90a01f0	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro Health Advanced Sensitive Relief	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	d7730674-7513-52cf-e053-2995a90ab32c	2026-01-08	Warnings	Exact identifier application number: M021
Kids Crest Bubblegum Flavor	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	26a7a892-5da4-4749-bbb6-566efab7d749	2026-01-08	Warnings	Exact identifier application number: M021
Crest Complete Multi-Benefit Plus Scope	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	8c91095d-88c0-4d22-a79a-7d0f0d05302b	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro Health Advanced Deep Clean Mint	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	d774295f-8ebd-9877-e053-2a95a90a9a0e	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
240698	sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse	PSN	e696038c-182e-4325-9b90-87fe498d9f67	8
240698	sodium fluoride 0.5 MG/ML Mouthwash	SCD	e696038c-182e-4325-9b90-87fe498d9f67	8
240698	sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse	SY	e696038c-182e-4325-9b90-87fe498d9f67	8

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
41163-213-44	41163021344	532 mL in 1 BOTTLE, PLASTIC (41163-213-44)	532 ml	2009-05-14	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Equaline 213.001/213AE rev 2 Anticavity Fluoride Rinse, Mint	United Natural Foods, Inc. dba UNFI \| Nice-Pak Products, LLC	2026-02-16	HUMAN OTC DRUG LABEL	8