Oral Antivavity

Product NDC: 41250-576
11-digit product format: 412500576
Labeler code: 41250
Product ID: 41250-576_4b33fb12-ad0a-8dd2-e063-6294a90a032b
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: 2015-02-06
Substance: SODIUM FLUORIDE
Active strength: .1 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: Oral Antivavity
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM FLUORIDE	.1 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
313029	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
af34f83f-1328-4897-9d04-72ca5a4101bf	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
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41250-576-86	Oral Antivavity	1000 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	1000		13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
CETYLPYRIDINIUM CHLORIDE	INACTIVE INGREDIENT	D9OM4SK49P	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
PHOSPHORIC ACID	INACTIVE INGREDIENT	E4GA8884NN	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
POLOXAMER 407	INACTIVE INGREDIENT	TUF2IVW3M2	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS	INACTIVE INGREDIENT	22ADO53M6F	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ORAL ANTIVAVITY (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
41250-576	ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC]	12	Current NDC, Legacy NDC, 1 package rows	20250423_af34f83f-1328-4897-9d04-72ca5a4101bf.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 30 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MIPasteOne Kids Blue Raspberry	MI PASTE ONE KIDS BLUE RASPBERRY	GC America Inc.	bf7d668c-752a-2eee-e053-2a95a90add16	2025-12-19	Warnings	Exact identifier application number: M021
MIPaste Plus Tutti Frutti	MIPASTE PLUS TUTTI FRUTTI	GC America Inc.	d724bd2a-2a8e-faeb-e053-2995a90aca19	2025-12-19	Warnings	Exact identifier application number: M021
MIPaste Plus Vanilla	MIPASTE PLUS VANILLA	GC America Inc.	d7244125-1ca5-78ba-e053-2995a90ab764	2025-12-19	Warnings	Exact identifier application number: M021
MIPaste Plus Melon	MIPASTE PLUS MELON	GC America Inc.	d724fe9f-c9ef-d9ad-e053-2995a90a7ecf	2025-12-19	Warnings	Exact identifier application number: M021
MIPaste Plus Mint	MIPASTE PLUS MINT	GC America Inc.	d72415b3-c501-141f-e053-2995a90aaaa3	2025-12-19	Warnings	Exact identifier application number: M021
MIPaste One Perio	MIPASTE ONE PERIO	GC America Inc.	d656b72d-48f8-4425-e053-2995a90ab1f2	2025-12-19	Warnings	Exact identifier application number: M021
MIPaste One Kids Blue Raspberry	MIPASTE ONE KIDS BLUE RASPBERRY	GC America Inc.	c07e1058-903b-fd47-e053-2995a90afdab	2025-12-19	Warnings	Exact identifier application number: M021
MIPaste Plus Strawberry	MIPASTE PLUS STRAWBERRY	GC America Inc.	d7235ad7-83d7-12e5-e053-2a95a90aaeaf	2025-12-19	Warnings	Exact identifier application number: M021
MIPaste One Kids Cotton Candy	MIPASTE ONE KIDS COTTON CANDY	GC America Inc.	c07d6b50-1d67-ea7f-e053-2a95a90afbe4	2025-12-19	Warnings	Exact identifier application number: M021
MIPaste One Kids Bubble Gum	MIPASTE ONE KIDS BUBBLE GUM	GC America Inc.	c07c7853-763b-4383-e053-2995a90ab725	2025-12-19	Warnings	Exact identifier application number: M021
MIPaste One	MIPASTE ONE	GC America Inc.	d71f8e6e-7005-4b3e-e053-2995a90a6789	2025-12-19	Warnings	Exact identifier application number: M021
TheraBreath AM-PM Twin Pack	SODIUM FLUORIDE	Church & Dwight Co., Inc.	4618e390-9039-a1d0-e063-6294a90ab294	2025-12-16	Warnings	Exact identifier application number: M021
Parodontax Gum Strengthen and Protect	STANNOUS FLUORIDE	Haleon US Holdings LLC	3bb40ceb-841b-4a25-e063-6294a90ab897	2025-12-15	Warnings	Exact identifier application number: M021
Sensodyne Pronamel Kids Bubble Mint	SODIUM FLUORIDE	Haleon US Holdings LLC	41b1e626-e79b-d638-e063-6394a90a1f5b	2025-12-15	Warnings	Exact identifier application number: M021
Simple Truth Kids Flouride	SODIUM MONOFLUOROPHOSPHATE	Kroger Company	82b9db89-d108-3f64-e053-2991aa0aee74	2025-12-15	Warnings	Exact identifier application number: M021
Natural Adult Fluoride	SODIUM MONOFLUOROPHOSPHATE	Kroger	a71c537e-39d9-1c3b-e053-2a95a90ac3ec	2025-12-15	Warnings	Exact identifier application number: M021
Therabreath Overnight Chamomile Mint	SODIUM FLUORIDE	Church & Dwight Co., Inc.	cc0c533c-145e-4877-b421-1baf3a3a572e	2025-12-11	Warnings	Exact identifier application number: M021
BRUSH BUDDIES CRAYOLA ANTICAVITY FLUORIDE BUBBLEGUM	SODIUM FLUORIDE	Kingkey MBC Life Technology Group co., LTD.	188d28f9-a814-0f98-e063-6294a90a106b	2025-12-11	Warnings	Exact identifier application number: M021
BRUSH BUDDIES CRAYOLA ANTICAVITY FLUORIDE WATERMELON	SODIUM FLUORIDE	Kingkey MBC Life Technology Group Co.,Ltd	1b4cf935-38a6-f4fb-e063-6394a90a4bc0	2025-12-11		Exact identifier application number: M021
BRUSH BUDDIES CRAYOLA ANTICAVITY FLUORIDE WATERMELON	SODIUM FLUORIDE	Kingkey MBC Life Technology Group co., LTD.	188cddb2-c799-0897-e063-6294a90a5d96	2025-12-11	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
313029	sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral Rinse	PSN	af34f83f-1328-4897-9d04-72ca5a4101bf	13
313029	sodium fluoride 0.2 MG/ML Mouthwash	SCD	af34f83f-1328-4897-9d04-72ca5a4101bf	13
313029	sodium fluoride 0.02 % (fluoride ion 0.009 % ) Oral Rinse	SY	af34f83f-1328-4897-9d04-72ca5a4101bf	13
313029	sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral Rinse	SY	af34f83f-1328-4897-9d04-72ca5a4101bf	13

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
41250-576-86	41250057686	1000 mL in 1 BOTTLE, PLASTIC (41250-576-86)	1000 ml	2015-02-06	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Meijer 576.001/576AC-AD Alcohol Free Fluoride Refreshing Mint Mouthwash	Meijer, Inc. \| Nice-Pak Products, LLC	2026-02-19	HUMAN OTC DRUG LABEL	13