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 40 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
WHITE GLO PROFESSIONAL CHOICE	SODIUM MONOFLUOROPHOSPHATE	WHITE GLO USA INC	13314c9a-de93-4f54-b703-b5cebdf1e6aa	2025-02-26	Warnings	Exact identifier application number: M021
WHITE GLO CHARCOAL	SODIUM MONOFLUOROPHOSPHATE	WHITE GLO USA INC	a14bb838-f07a-3a6f-e053-2995a90a535d	2025-02-26	Warnings	Exact identifier application number: M021
White Glo Maximum White Charcoal	SODIUM MONOFLUOROPHOSPHATE	WHITE GLO USA INC	ce4f64d2-969f-7ac1-e053-2995a90a627b	2025-02-26	Warnings	Exact identifier application number: M021
White Glo Instant White	SODIUM MONOFLUOROPHOSPHATE	WHITE GLO USA INC	ce4f0f8f-46f0-b4e6-e053-2a95a90af6c6	2025-02-26	Warnings	Exact identifier application number: M021
White Glo Instant White Blue Foam Optical Enhancers Fluoride Anticavity Value 2 pack and Toothbrush	SODIUM MONOFLUOROPHOSPHATE	WHITE GLO USA INC	7c15eedb-d4ca-4fc1-8a1e-6f9cad0cc126	2025-02-26	Warnings	Exact identifier application number: M021
White Glo Mouthwash Protection	SODIUM MONOFLUOROPHOSPHATE	WHITE GLO USA INC	ce4f0f8f-46f1-b4e6-e053-2a95a90af6c6	2025-02-26	Warnings	Exact identifier application number: M021
White Glo Professional White AntiCavity	SODIUM MONOFLUOROPHOSPHATE	WHITE GLO USA INC	1fb04108-31b3-43dd-9509-bfa846113516	2025-02-26	Warnings	Exact identifier application number: M021
White Glo Activated Charcoal Twin Pack	SODIUM FLUORIDE	WHITE GLO USA INC	6adaca4f-5599-41e0-9215-c7ee5c1dc372	2025-02-26	Warnings	Exact identifier application number: M021
White Glo Professional Choice Twin Pack	SODIUM FLUORIDE	WHITE GLO USA INC	0c913e38-e655-7208-e063-6294a90a58c9	2025-02-26	Warnings	Exact identifier application number: M021
White Glo Advantage Anticavity Fluoride Purple	SODIUM MONOFLUOROPHOSPHATE	WHITE GLO USA INC	b25aa35b-98ce-4605-a7b1-8c2fe476e1a8	2025-02-26	Warnings	Exact identifier application number: M021
White Glo Coffee and Tea Stain Remover Fluoride Anticavity	SODIUM MONOFLUOROPHOSPHATE	WHITE GLO USA INC	d69387f9-03b8-4551-a814-20606500af28	2025-02-26	Warnings	Exact identifier application number: M021
White Glo Advantage Anticavity Professional Whitening	SODIUM MONOFLUOROPHOSPHATE	WHITE GLO USA INC	164c3e87-74e5-4128-9bd7-60e162e58984	2025-02-26	Warnings	Exact identifier application number: M021
Listerine Total Care Kids Anticavity Fluoride Rinse Mint Shield	SODIUM FLUORIDE	Kenvue Brands LLC	2e01b69a-b8f7-f2b9-e063-6294a90af388	2025-02-13	Warnings	Exact identifier application number: M021
Listerine Total Care Kids Anticavity Fluoride Rinse Bubble Blast	SODIUM FLUORIDE	Kenvue Brands LLC	2e021015-bb43-482b-e063-6294a90a6902	2025-02-13	Warnings	Exact identifier application number: M021
ZONSEN Gel Fluoride	GEL FLUORIDE TOOTHPASTE	Wuhan Zonsen Medical Products Co., Ltd.	2c1e40c9-8314-46ac-e063-6294a90a84ba	2025-02-11	Warnings	Exact identifier application number: M021
ZONSEN Toothpaste,white	TOOTHPASTE	Wuhan Zonsen Medical Products Co., Ltd.	2c3349bf-710b-fb84-e063-6394a90a3cc7	2025-02-11	Warnings	Exact identifier application number: M021
DawnMist	TOOTHPASTE	Dukal LLC	147f7738-5080-9907-e063-6294a90a6170	2025-02-07	Warnings	Exact identifier application number: M021
DawnMist Gel Fluoride	GEL FLUORIDE TOOTHPASTE	Dukal LLC	14443184-1694-70b9-e063-6394a90a86fe	2025-02-07	Warnings	Exact identifier application number: M021
Quip Anticavity Fluoride Concentrate	SODIUM FLUORIDE	Quip NYC Inc.	b3da65bb-0871-34e7-e053-2a95a90a310e	2025-01-30	Warnings	Exact identifier application number: M021
Quip Anticavity	SODIUM FLUORIDE	Quip NYC Inc.	b6d4cfe3-535e-9163-e053-2a95a90ae140	2025-01-30	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