Mouth Rinse

Product NDC: 0363-0163
11-digit product format: 003630163
Labeler code: 0363
Product ID: 0363-0163_4aa46dbb-3e7c-cd84-e063-6394a90ad744
Type: HUMAN OTC DRUG
Nonproprietary name: sodium fluoride
Dosage form: MOUTHWASH
Route: ORAL
Labeler: Walgreen Co.
Application: M021
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2006-03-15
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: Mouth Rinse
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
1038904	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
eae87899-3eba-4d50-bc31-9eaf54ff9e00	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
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0363-0163-86	2023-10-13	C162847	48780-1	f386c649-e915-0266-e053-dadaa90a7c1a	Walgreens 163.005/163AF-AG Anticavity Mouth Rinse
0363-0163-86	2023-01-30	C162847	48780-1	f386c649-e915-0266-e053-dadaa90a7c1a	Walgreens 163.005/163AF-AG Anticavity Mouth Rinse

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0363-0163-86	Mouth Rinse	1000 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	1000		16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
PHOSPHORIC ACID	INACTIVE INGREDIENT	E4GA8884NN	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
POLOXAMER 407	INACTIVE INGREDIENT	TUF2IVW3M2	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
SODIUM PHOSPHATE, DIBASIC	INACTIVE INGREDIENT	GR686LBA74	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
SORBITOL	INACTIVE INGREDIENT	506T60A25R	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
SUCRALOSE	INACTIVE INGREDIENT	96K6UQ3ZD4	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-0163	MOUTH RINSE (SODIUM FLUORIDE) MOUTHWASH [WALGREEN]	14	Current NDC, Legacy NDC, 1 package rows	20240716_eae87899-3eba-4d50-bc31-9eaf54ff9e00.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 27 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Crest plus Tartar Protection Whitening	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	08776dfc-b07a-3729-e063-6394a90aeeed	2026-01-08	Warnings	Exact identifier application number: M021
Crest Plus Active Fresh plus Whitening Scope	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	17f3b749-01ea-2561-e063-6294a90a5d3b	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Advanced Deep Clean	SODIUM FLUORIDE	Procter & Gamble Manfuacturing Company	128613c4-c06b-bdf5-e063-6294a90acd34	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Brilliance Pro Rinse	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	13a01190-a6f3-17b3-e063-6294a90a36c2	2026-01-08	Warnings	Exact identifier application number: M021
HEB HEBuddy	FLUORIDE	HEB	2c972c65-34aa-4348-b997-c5e65a884575	2026-01-08	Warnings	Exact identifier application number: M021
ARC 2 in 1 Whitening and Anticavity	SODIUM MONOFLUOROPHOSPHATE	The Procter & Gamble Manufacturing Company	12634efa-35e3-76d7-e063-6294a90a3de4	2026-01-08		Exact identifier application number: M021
Crest Plus Whitening Deep Clean	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	15482445-39f3-7e02-e063-6294a90ad1dc	2026-01-08	Warnings	Exact identifier application number: M021
H E B Restore and Defend	FLUORIDE	HEB	56080493-9ab8-4b4f-be5f-7df22dee133f	2026-01-08	Warnings	Exact identifier application number: M021
Crest Plus Cinnamon Expressions plus Whitening	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	151d2a0a-448f-7744-e063-6294a90acd3b	2026-01-08	Warnings	Exact identifier application number: M021
Oral B Mouth Sore Special Care Rinse	HYDROGEN PEROXIDE	The Procter & Gamble Manufacturing Company	22e2dc15-5794-28ed-e063-6394a90a36d3	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro-Health Advanced Anti-Cavity Max Cavity	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	15d70b80-3b25-bc32-e063-6394a90a163e	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Brilliance Bright Mint	SODIUM FLUORIDE	Procter & Gamble Manfuacturing Company	1dee0584-0fed-61c6-e063-6394a90adbcd	2026-01-08	Warnings	Exact identifier application number: M021
HEB Gleaming White Arctic Mint	SODIUM FLUORIDE	HEB	8248eddb-20a5-7084-e053-2991aa0a16b5	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro-Health Gum Rescue Pro Soothing Clean	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	2f10c7ac-eb60-011e-e063-6394a90aca13	2026-01-08	Warnings	Exact identifier application number: M021
Crest Deep Cleanse Cavity Defense	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	2e09cb3b-cf59-15b1-e063-6394a90a5c6a	2026-01-08	Warnings	Exact identifier application number: M021
Crest Pro-Health Maximum Cavity Protection	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	2eaeddc5-1559-9378-e063-6394a90a4ed7	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Deep Stain Remover Dazzling Mint	SODIUM MONOFLUOROPHOSPHATE	The Procter & Gamble Manufacturing Company	2f11e935-1711-5f1a-e063-6294a90af7d8	2026-01-08		Exact identifier application number: M021
HEB Gleaming White Fresh Mint	SODIUM FLUORIDE	HEB	82491c8f-d2c2-2e4a-e053-2a91aa0a572f	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Brilliance Pro Ultra White	SODIUM MONOFLUOROPHOSPHATE	The Procter & Gamble Manufacturing Company	338acdf2-548c-0614-e063-6294a90af635	2026-01-08		Exact identifier application number: M021
KIDS Crest Advanced Sugar and Bacteria Shield	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	2f371af0-a2d4-25a6-e063-6394a90a923d	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
1038904	sodium fluoride 0.0221 % (fluoride ion 0.01 % ) Mouthwash	PSN	eae87899-3eba-4d50-bc31-9eaf54ff9e00	16
1038904	sodium fluoride 0.221 MG/ML Mouthwash	SCD	eae87899-3eba-4d50-bc31-9eaf54ff9e00	16
1038904	sodium fluoride 0.0221 % (fluoride 0.01 % ) Oral Rinse	SY	eae87899-3eba-4d50-bc31-9eaf54ff9e00	16

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0363-0163-86	00363016386	1000 mL in 1 BOTTLE, PLASTIC (0363-0163-86)	1000 ml	2006-03-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Walgreens 163.005/163AF-AG Anticavity Mouth Rinse	Walgreen Co. \| Nice-Pak Products, LLC	2026-02-12	HUMAN OTC DRUG LABEL	16