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 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
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