Alcohol-Free Anticavity

Product NDC: 41250-482
11-digit product format: 412500482
Labeler code: 41250
Product ID: 41250-482_4b33e88d-834a-6e98-e063-6294a90a37a4
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium fluoride
Dosage form: LIQUID
Route: ORAL
Labeler: Meijer, Inc.
Application: M021
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2012-02-22
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: Alcohol-Free Anticavity
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
c4dcb1d8-f2af-4363-8fcd-c7d1197d66ea	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
41250-482-86	Alcohol-Free Anticavity	1000 mL in 1 BOTTLE, PLASTIC	LIQUID	1000		15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
CETYLPYRIDINIUM CHLORIDE	INACTIVE INGREDIENT	D9OM4SK49P	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
D&C RED NO. 33	INACTIVE INGREDIENT	9DBA0SBB0L	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
FD&C GREEN NO. 3	INACTIVE INGREDIENT	3P3ONR6O1S	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
PHOSPHORIC ACID	INACTIVE INGREDIENT	E4GA8884NN	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
POLOXAMER 407	INACTIVE INGREDIENT	TUF2IVW3M2	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
SACCHARIN SODIUM DIHYDRATE	INACTIVE INGREDIENT	SB8ZUX40TY	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS	INACTIVE INGREDIENT	22ADO53M6F	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1
water	INACTIVE INGREDIENT	059QF0KO0R	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41250-482	ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [MEIJER DISTRIBUTION, INC]	13	Current NDC, Legacy NDC, 1 package rows	20240719_c4dcb1d8-f2af-4363-8fcd-c7d1197d66ea.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 6 of 51 · 1,013 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Freshen Up	SODIUM FLUORIDE, POTASSIUM NITRATE	MKJ BRANDS LLC	476f453b-9215-0a11-e063-6294a90a5cd4	2026-07-14	Warnings	Exact identifier application number: M021
Freshen Up Vanilla Mint	SODIUM FLUORIDE	MKJ BRANDS LLC	525662da-42be-eaa6-e063-6294a90af110	2026-07-14	Warnings	Exact identifier application number: M021
Freshen Up twisted peppermint	SODIUM FLUORIDE	MKJ BRANDS LLC	526acbdd-6531-692d-e063-6394a90ab9f1	2026-07-14	Warnings	Exact identifier application number: M021
Freshen Up chai latte mint	SODIUM FLUORIDE	MKJ BRANDS LLC	52e364f9-113a-df4e-e063-6294a90a263b	2026-07-14	Warnings	Exact identifier application number: M021
Freshen Up Holiday mint	SODIUM FLUORIDE	MKJ BRANDS LLC	5257c409-d379-8c48-e063-6294a90acda9	2026-07-14	Warnings	Exact identifier application number: M021
Freshen-up Matcha Mint	SODIUM FLUORIDE	MKJ BRANDS LLC	52bbc6d9-17ab-851a-e063-6394a90ab4bf	2026-07-14	Warnings	Exact identifier application number: M021
Freshen Up pepper mint	SODIUM FLUORIDE	MKJ BRANDS LLC	5259bc45-85da-b17b-e063-6294a90a7919	2026-07-14	Warnings	Exact identifier application number: M021
Colgate Optic White Advanced Icy Fresh	SODIUM MONOFLUOROPHOSPHATE	Colgate-Palmolive Company	f95496e3-11ec-4cd6-b3ee-cf6c657b790b	2026-07-13	Warnings	Exact identifier application number: M021
COLGATE MAX FRESH COCONUT PINEAPPLE	SODIUM FLUORIDE	Colgate-Palmolive Company	7f240d1d-ea3d-42b1-a4b0-106c58707452	2026-07-08	Warnings	Exact identifier application number: M021
Crest 3D White Deep Stain Remover Ultra White	SODIUM MONOFLUOROPHOSPHATE	The Procter & Gamble Manufacturing Company	2f24a9eb-7a89-30e1-e063-6394a90a032b	2026-07-08		Exact identifier application number: M021
Dr. Noah Kids Tooth	SODIUM MONOFLUOROPHOSPHATE	Project Noah Inc.	562311aa-9ac5-00c2-e063-6394a90a67a7	2026-07-08	Warnings	Exact identifier application number: M021
COLGATE BAKING SODA AND PEROXIDE WHITENING OXYGEN BUBBLES FROSTY MINT	SODIUM MONOFLUOROPHOSPHATE	Colgate-Palmolive Company	263fef13-347b-489b-987d-933a63dbc900	2026-07-08	Warnings	Exact identifier application number: M021
Colgate Triple Action	SODIUM FLUORIDE	Colgate-Palmolive Company	3082e9ba-66d9-4fc7-bbe6-b41b60939bd2	2026-07-08	Warnings	Exact identifier application number: M021
Colgate Junior Kids Batman Mild Bubble Fruit Fluoride	SODIUM FLUORIDE	Colgate-Palmolive Company	f464cecb-e876-4057-ab5c-94de747434db	2026-07-08	Warnings	Exact identifier application number: M021
Crest Premium Plus Scope Active Foam plus Whitening Minty Fresh	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	560815d6-018a-0c24-e063-6394a90a1071	2026-07-07	Warnings	Exact identifier application number: M021
Crest Plus Scope plus Whitening with Mouthwash	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	54ecfbed-ba99-11eb-e063-6294a90ae64d	2026-07-07	Warnings	Exact identifier application number: M021
Crest Plus Scope plus Whitening Minty Fresh with Mouthwash striped	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	56091601-74dd-0a3b-e063-6394a90af476	2026-07-07	Warnings	Exact identifier application number: M021
Crest Plus Scope plus Whitening Outlast Mint	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	55054217-f21b-1c41-e063-6394a90ae40b	2026-07-07	Warnings	Exact identifier application number: M021
Hello Dragon Dazzle Dragon Dazzle Fluoride	SODIUM FLUORIDE	Colgate-Palmolive Company	eaca1ad1-9e31-b904-4148-247ad2460661	2026-07-07	Warnings	Exact identifier application number: M021
Colgate Cavity Protection	SODIUM FLUORIDE	Colgate-Palmolive Company	cdd2ad04-8c65-40f2-b323-5ce11af52e4f	2026-07-06	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	c4dcb1d8-f2af-4363-8fcd-c7d1197d66ea	15
313029	sodium fluoride 0.2 MG/ML Mouthwash	SCD	c4dcb1d8-f2af-4363-8fcd-c7d1197d66ea	15
313029	sodium fluoride 0.02 % (fluoride ion 0.009 % ) Oral Rinse	SY	c4dcb1d8-f2af-4363-8fcd-c7d1197d66ea	15
313029	sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral Rinse	SY	c4dcb1d8-f2af-4363-8fcd-c7d1197d66ea	15

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
41250-482-86	41250048286	1000 mL in 1 BOTTLE, PLASTIC (41250-482-86)	1000 ml	2012-02-22	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Meijer 482.002/482AC Alcohol Free Fluoride Violet Mint Mouthwash	Meijer, Inc. \| Nice-Pak Products, LLC	2026-02-19	HUMAN OTC DRUG LABEL	15