ANTI CAVITY FLUORIDE

Product NDC: 52000-107
11-digit product format: 520000107
Labeler code: 52000
Product ID: 52000-107_69e7d7f5-a88f-4067-b25e-0b7ab646044f
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Monofluorophosphate
Dosage form: PASTE
Route: DENTAL
Labeler: Universal Distribution Center LLC
Application: M021
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-05-15
Substance: SODIUM MONOFLUOROPHOSPHATE
Active strength: .76 g/100g
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: ANTI CAVITY FLUORIDE
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM MONOFLUOROPHOSPHATE	.76 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
C810JCZ56Q	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
545626	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
421fc2f0-b118-4e7a-a399-ba4780028c54	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52000-107-01	ANTI CAVITY FLUORIDE	181 g in 1 TUBE	PASTE	181		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52000-107	ANTI CAVITY FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE [UNIVERSAL DISTRIBUTION CENTER LLC]	2	Current NDC, Legacy NDC, 1 package rows	20231121_421fc2f0-b118-4e7a-a399-ba4780028c54.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 49 · 974 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
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
Crest Pro-Health Gum Detoxify Plus	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	2f9e346e-d664-81d5-e063-6394a90a4525	2026-01-08	Warnings	Exact identifier application number: M021
Crest 3D White Holiday Smile Deep Stain Remover and Whitestrips	SODIUM MONOFLUOROPHOSPHATE	The Procter & Gamble Manufacturing Company	3c57d487-a3c7-b238-e063-6294a90aed81	2026-01-08		Exact identifier application number: M021
Crest Complete plus Scope Pro Advanced Freshness	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	325c3ab2-aaa2-a06f-e063-6294a90abefb	2026-01-08	Warnings	Exact identifier application number: M021
Crest Tartar Protection	SODIUM FLUORIDE	Procter & Gamble Manufactura, S. de R.L. de C.V.	5940711d-71b7-cb7d-e053-2a91aa0aef18	2026-01-08	Warnings	Exact identifier application number: M021
Meijer Restore and Defend Sensitive	STANNOUS FLUORIDE	Meijer Distribution Inc	82bdfdb5-39f2-8c09-e053-2991aa0a096c	2026-01-08	Warnings	Exact identifier application number: M021

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
C810JCZ56Q	SODIUM MONOFLUOROPHOSPHATE	10163-15-2	SODIUM MONOFLUOROPHOSPHATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
545626	sodium monofluorophosphate 0.76 % Toothpaste	PSN	421fc2f0-b118-4e7a-a399-ba4780028c54	2
545626	sodium monofluorophosphate 0.0076 MG/MG Toothpaste	SCD	421fc2f0-b118-4e7a-a399-ba4780028c54	2
545626	sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste	SY	421fc2f0-b118-4e7a-a399-ba4780028c54	2
545626	sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste	SY	421fc2f0-b118-4e7a-a399-ba4780028c54	2
545626	sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )Toothpaste	SY	421fc2f0-b118-4e7a-a399-ba4780028c54	2
545626	sodium monofluorophosphate 0.76 % (fluoride ion 0.15 % )Toothpaste	SY	421fc2f0-b118-4e7a-a399-ba4780028c54	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
52000-107-01	52000010701	181 g in 1 TUBE (52000-107-01)	181 g	2020-05-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
UNIVERSAL ANTI-CAVITY FLUORIDE TOOTHPASTE	Universal Distribution Center LLC	2023-11-16	HUMAN OTC DRUG LABEL	2