Pro-Den Rx

Product NDC
59883-720
11-digit product format
598830720
Labeler code
59883
Product ID
59883-720_0a95fcbe-e811-031d-e063-6294a90aec1b
Type
HUMAN OTC DRUG
Nonproprietary name
Stannous Fluoride
Dosage form
RINSE
Route
ORAL
Labeler
Den-mat Holdings, Llc
Application
M021
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2008-10-31
Substance
STANNOUS FLUORIDE
Active strength
1.53 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
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
Pro-Den Rx
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
STANNOUS FLUORIDE1.53 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3FTR44B32QInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9036aa8a-59b1-41b0-b3cb-529d3303a1c0Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59883-720-08Pro-Den Rx283.5 g in 1 BOTTLERINSE283.56
59883-720-08Pro-Den Rx1 in 1 CARTONRINSE16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
STANNOUS FLUORIDEACTIVE INGREDIENT3FTR44B32QPRO-DEN RX (SODIUM FLUORIDE) GEL [ZILA THERAPEUTICS, INC.]1
FLUORIDE IONACTIVE MOIETYQ80VPU408OPRO-DEN RX (SODIUM FLUORIDE) GEL [ZILA THERAPEUTICS, INC.]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXPRO-DEN RX (SODIUM FLUORIDE) GEL [ZILA THERAPEUTICS, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59883-720PRO-DEN RX (STANNOUS FLUORIDE) RINSE [DEN-MAT HOLDINGS, LLC]6Current NDC, Legacy NDC, 2 package rows20231216_9036aa8a-59b1-41b0-b3cb-529d3303a1c0.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 30 of 50 · 995 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MIPasteOne Kids Blue RaspberryMI PASTE ONE KIDS BLUE RASPBERRYGC America Inc.bf7d668c-752a-2eee-e053-2a95a90add162025-12-19WarningsExact identifier
application number: M021
MIPaste Plus Tutti FruttiMIPASTE PLUS TUTTI FRUTTIGC America Inc.d724bd2a-2a8e-faeb-e053-2995a90aca192025-12-19WarningsExact identifier
application number: M021
MIPaste Plus VanillaMIPASTE PLUS VANILLAGC America Inc.d7244125-1ca5-78ba-e053-2995a90ab7642025-12-19WarningsExact identifier
application number: M021
MIPaste Plus MelonMIPASTE PLUS MELONGC America Inc.d724fe9f-c9ef-d9ad-e053-2995a90a7ecf2025-12-19WarningsExact identifier
application number: M021
MIPaste Plus MintMIPASTE PLUS MINTGC America Inc.d72415b3-c501-141f-e053-2995a90aaaa32025-12-19WarningsExact identifier
application number: M021
MIPaste One PerioMIPASTE ONE PERIOGC America Inc.d656b72d-48f8-4425-e053-2995a90ab1f22025-12-19WarningsExact identifier
application number: M021
MIPaste One Kids Blue RaspberryMIPASTE ONE KIDS BLUE RASPBERRYGC America Inc.c07e1058-903b-fd47-e053-2995a90afdab2025-12-19WarningsExact identifier
application number: M021
MIPaste Plus StrawberryMIPASTE PLUS STRAWBERRYGC America Inc.d7235ad7-83d7-12e5-e053-2a95a90aaeaf2025-12-19WarningsExact identifier
application number: M021
MIPaste One Kids Cotton CandyMIPASTE ONE KIDS COTTON CANDYGC America Inc.c07d6b50-1d67-ea7f-e053-2a95a90afbe42025-12-19WarningsExact identifier
application number: M021
MIPaste One Kids Bubble GumMIPASTE ONE KIDS BUBBLE GUMGC America Inc.c07c7853-763b-4383-e053-2995a90ab7252025-12-19WarningsExact identifier
application number: M021
MIPaste OneMIPASTE ONEGC America Inc.d71f8e6e-7005-4b3e-e053-2995a90a67892025-12-19WarningsExact identifier
application number: M021
TheraBreath AM-PM Twin PackSODIUM FLUORIDEChurch & Dwight Co., Inc.4618e390-9039-a1d0-e063-6294a90ab2942025-12-16WarningsExact identifier
application number: M021
Parodontax Gum Strengthen and ProtectSTANNOUS FLUORIDEHaleon US Holdings LLC3bb40ceb-841b-4a25-e063-6294a90ab8972025-12-15WarningsExact identifier
application number: M021
Sensodyne Pronamel Kids Bubble MintSODIUM FLUORIDEHaleon US Holdings LLC41b1e626-e79b-d638-e063-6394a90a1f5b2025-12-15WarningsExact identifier
application number: M021
Simple Truth Kids FlourideSODIUM MONOFLUOROPHOSPHATEKroger Company82b9db89-d108-3f64-e053-2991aa0aee742025-12-15WarningsExact identifier
application number: M021
Natural Adult FluorideSODIUM MONOFLUOROPHOSPHATEKrogera71c537e-39d9-1c3b-e053-2a95a90ac3ec2025-12-15WarningsExact identifier
application number: M021
Therabreath Overnight Chamomile MintSODIUM FLUORIDEChurch & Dwight Co., Inc.cc0c533c-145e-4877-b421-1baf3a3a572e2025-12-11WarningsExact identifier
application number: M021
BRUSH BUDDIES CRAYOLA ANTICAVITY FLUORIDE BUBBLEGUMSODIUM FLUORIDEKingkey MBC Life Technology Group co., LTD.188d28f9-a814-0f98-e063-6294a90a106b2025-12-11WarningsExact identifier
application number: M021
BRUSH BUDDIES CRAYOLA ANTICAVITY FLUORIDE WATERMELONSODIUM FLUORIDEKingkey MBC Life Technology Group Co.,Ltd1b4cf935-38a6-f4fb-e063-6394a90a4bc02025-12-11Exact identifier
application number: M021
BRUSH BUDDIES CRAYOLA ANTICAVITY FLUORIDE WATERMELONSODIUM FLUORIDEKingkey MBC Life Technology Group co., LTD.188cddb2-c799-0897-e063-6294a90a5d962025-12-11WarningsExact identifier
application number: M021

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59883-720-08598830720081 BOTTLE in 1 CARTON (59883-720-08) / 283.5 g in 1 BOTTLE1 bottle2008-10-310000-00-00NoNoCurrent