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 9 of 51 · 1,013 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Optimax Anticavity Fluoride Raspberry	SODIUM MONOFLUOROPHOSPHATE	White Glo USA Inc	57e1d1cb-da58-4cd2-b960-4056e0b0d214	2026-06-05	Warnings	Exact identifier application number: M021
3ECARE Dual FormulaWhiteningToothpaste	SODIUM FLUORIDE	Hangzhou Namei Zhikang Technology Co., Ltd.	533fb7dd-7f84-59c5-e063-6394a90accad	2026-06-02	Warnings	Exact identifier application number: M021
3ECARE Dual FormulaToothpastefor sensitiveteeth	POTASSIUM NITRATE SODIUM MONOFLUOROPHOSPHATE	Hangzhou Namei Zhikang Technology Co., Ltd.	533fc83e-a8cf-15c1-e063-6294a90a7b74	2026-06-02	Warnings	Exact identifier application number: M021
Walgreens Restore and Defend	STANNOUS FLUORIDE	Walgreens	e808ea4b-9081-085b-e053-2a95a90a4f9b	2026-06-02	Warnings	Exact identifier application number: M021
Hello Unicorn Splash unicorn splash anticavity fluoride rinse	SODIUM FLUORIDE	Colgate-Palmolive Company	a1014431-7d23-aaff-6dc7-ab58683d0338	2026-06-02	Warnings	Exact identifier application number: M021
Therabreath Anticavity	SODIUM FLUORIDE	Church & Dwight Co., Inc.	feab3d45-ff95-4b32-8258-7d932a7380c9	2026-06-01	Warnings	Exact identifier application number: M021
Orajel Toy Story 5 Anticavity	SODIUM FLUORIDE	Church & Dwight Co., Inc.	4b80947d-f389-2f80-e063-6294a90abd55	2026-06-01	Warnings	Exact identifier application number: M021
Arm and Hammer	SODIUM FLUORIDE	Church & Dwight Co., Inc.	54113245-0c1e-739e-e063-6294a90aea42	2026-06-01	Warnings	Exact identifier application number: M021
Arm and Hammer	SODIUM FLUORIDE	Church & Dwight Co., Inc.	545258fd-8179-fffc-e063-6394a90a467f	2026-06-01	Warnings	Exact identifier application number: M021
Orajel Paw Patrol	SODIUM FLUORIDE	Church & Dwight Co., Inc.	99d87bea-3e99-5d04-e053-2a95a90aaf54	2026-06-01	Warnings	Exact identifier application number: M021
Orajel SuperMario	ANTICAVITY TOOTHPASTE	Church & Dwight Co., Inc.	27d2f6cb-8661-da9c-e063-6394a90a5bde	2026-06-01	Warnings	Exact identifier application number: M021
Orajel KidsToothpaste	SODIUM FLUORIDE	Church & Dwight Co., Inc.	99d62125-c2c5-5926-e053-2995a90aaa29	2026-06-01	Warnings	Exact identifier application number: M021
AIM CAVITY PROTECTION Multi Benefit	SODIUM FLUORIDE	Church & Dwight Co., Inc.	1d0f8a33-0b01-40e2-e054-00144ff88e88	2026-06-01	Warnings	Exact identifier application number: M021
Crest plus Tartar Protection Whitening	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	560980ea-749f-593d-e063-6394a90a1b9e	2026-06-01	Warnings	Exact identifier application number: M021
Colgate Revitalizing White	SODIUM MONOFLUOROPHOSPHATE	Colgate-Palmolive Company	c67223ae-b068-41c5-a15b-7ae9840b93ef	2026-05-27	Warnings	Exact identifier application number: M021
Colgate Kids Harry Potter	SODIUM FLUORIDE	Colgate-Palmolive Company	61c06da4-9f02-4fbc-b80f-1c443e298496	2026-05-26	Warnings	Exact identifier application number: M021
sodium fluoride rinse	SODIUM FLUORIDE RINSE	Rockland Cosmetics, Inc.	52430b12-4d5f-d1e1-e063-6394a90abd64	2026-05-20	Warnings, Adverse reactions	Exact identifier application number: M021
Anticavity	SODIUM FLUORIDE	H E B	d0a52519-3339-40ea-93e5-78f76d348a4d	2026-05-14	Warnings, Adverse reactions	Exact identifier application number: M021
Burts Bees Extra White	SODIUM FLUORIDE	Procter & Gamble Manufacturing Company	c92524fd-8b93-592d-e053-2a95a90a88c6	2026-05-13	Warnings	Exact identifier application number: M021
MIPaste Plus Strawberry	SODIUM FLUORIDE	GC America Inc.	1b68bd67-65d3-4c64-e054-00144ff8d46c	2026-05-12	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