Anticavity Rinse

Product NDC: 41250-004
11-digit product format: 412500004
Labeler code: 41250
Product ID: 41250-004_4b318df0-16aa-afb2-e063-6394a90ace68
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Fluoride
Dosage form: MOUTHWASH
Route: ORAL
Labeler: Meijer, Inc.
Application: M021
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2002-06-27
Substance: SODIUM FLUORIDE
Active strength: .2 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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 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
001777fb-196c-499a-94c8-6cdcef0958e9	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
777d68c6-a5ab-e06c-d314-677b0b9af0c8	Product name	2	20240508
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717
6084a4f4-5437-c9a5-caec-5361ee075a59	Product name	1	20140508
90c5639a-61b0-88d6-ddcf-21888e94869a	Product name	1	20140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877	Product name	1	20140508
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41250-004-44	Anticavity Rinse	532 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	532		19

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	1
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	1
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	1
CETYLPYRIDINIUM CHLORIDE	INACTIVE INGREDIENT	D9OM4SK49P	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	1
POLOXAMER 407	INACTIVE INGREDIENT	TUF2IVW3M2	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	1
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	1
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	1
SODIUM PHOSPHATE	INACTIVE INGREDIENT	SE337SVY37	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41250-004	ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.]	18	Current NDC, Legacy NDC, 1 package rows	20250311_001777fb-196c-499a-94c8-6cdcef0958e9.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 12 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Crest Clean Breath Peppermint	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	4f1ef07b-ee68-e6ae-e063-6394a90af5e5	2026-04-10	Warnings	Exact identifier application number: M021
Crest Clean Breath Spearmint	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	4f20343e-6c03-48e8-e063-6294a90a8cdf	2026-04-10	Warnings	Exact identifier application number: M021
Crest Clean Breath Smooth Mint	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	4f2042b4-8eae-5c2c-e063-6394a90a640c	2026-04-10	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Arctic Fresh with Stain-Blasting Foam	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	4ef4146d-6281-fe66-e063-6394a90a32c3	2026-04-09	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Glamorous White with Stain-Blasting Foam	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	4ef5261e-9d2f-ae05-e063-6294a90a489a	2026-04-09	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Luminous Mint Daily Whitening Upkeep	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	4f0876d9-41c9-d891-e063-6394a90a1cbd	2026-04-09	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Charcoal with Stain-Blasting Foam	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	4ef57a05-b9f5-42f7-e063-6294a90a5d89	2026-04-09	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Radiant Mint with Stain Blasting Foam	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	4ee26a82-16fd-f0fb-e063-6394a90a91d1	2026-04-09	Warnings	Exact identifier application number: M021
Crest 3D White Whitening Therapy Deep Clean Charcoal	SODIUM FLUORIDE	Procter & Gamble Manfuacturing Company	812c1519-1a4b-2495-e053-2a91aa0a914a	2026-04-09	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Deep Clean with Stain-Blasting Foam	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	4ef4e7c2-1f58-59fc-e063-6294a90ad43b	2026-04-08	Warnings	Exact identifier application number: M021
Anticavity mouth rinse Low-foaming Spearmint	779 US VARIANT ANTICAVITY MOUTH RINSE LOW-FOAMING SPEARMINT	Dyson Technology Limited	4ef669b9-defe-8965-e063-6394a90ab335	2026-04-08	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Radiant Mint	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	f5c89efc-5fa0-2a05-e053-2a95a90a7b9c	2026-04-07	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Charcoal	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	f4eb8111-53da-17ae-e053-2a95a90a1127	2026-04-07	Warnings	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	ADUSA Distribution, LLC	35385ada-bd8d-4d38-9587-0256885f749f	2026-04-07	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	ADUSA Distribution, LLC	cf0c8b48-0d1c-406a-a67d-7d16187d38d8	2026-04-07	Warnings, Adverse reactions	Exact identifier application number: M021
Crest 3D White Arctic Fresh	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	fa08a877-b9e5-4eba-b832-3a28f4f3f83c	2026-04-07	Warnings	Exact identifier application number: M021
Anticavity Fluoride	SODIUM FLUORIDE	Family Dollar (FAMILY WELLNESS)	63c4c0e9-84b1-4076-bdf4-7e9543b2cf46	2026-04-01	Warnings	Exact identifier application number: M021
CloSYS Silver Sensitive Mouth Rinse Fluoride Rinse	SODIUM FLUORIDE	Rowpar Pharmaceuticals, Inc.	98a8cee8-9f3c-4a4a-89f8-72e1f1b06796	2026-04-01	Warnings	Exact identifier application number: M021
CloSYS	SODIUM FLUORIDE	Rowpar Pharmaceuticals, Inc.	5f87abb7-0e9d-6369-e053-2a91aa0a2411	2026-03-31	Warnings	Exact identifier application number: M021
Crest Clean Breath Spearmint	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	4e544d09-0cf3-f0c7-e063-6394a90a2369	2026-03-31	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	001777fb-196c-499a-94c8-6cdcef0958e9	19
240698	sodium fluoride 0.5 MG/ML Mouthwash	SCD	001777fb-196c-499a-94c8-6cdcef0958e9	19
240698	sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse	SY	001777fb-196c-499a-94c8-6cdcef0958e9	19

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
41250-004-44	41250000444	532 mL in 1 BOTTLE, PLASTIC (41250-004-44)	532 ml	2002-06-27	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Meijer 004.002/004AE Anticavity Fluoride Rinse, Bubble Gum	Meijer, Inc. \| Nice-Pak Products, LLC	2026-02-19	HUMAN OTC DRUG LABEL	19