FDA.reportPublic FDA data

Super Mint Prescription

Product NDC
83729-102
11-digit product format
837290102
Labeler code
83729
Product ID
83729-102_c645431b-c217-493c-b5df-7df81f2d9e1d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Anticavity Toothpaste
Dosage form
PASTE, DENTIFRICE
Route
DENTAL
Labeler
SuperMouth, LLC.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2023-10-13
Substance
SODIUM FLUORIDE
Active strength
1.1 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Super Mint Prescription
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM FLUORIDE1.1 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8ZYQ1474W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
392038Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
6773eb58-93b0-4e86-b780-7dde378c0bc3Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83729-102-10Super Mint Prescription96 g in 1 TUBEPASTE, DENTIFRICE963
83729-102-10Super Mint Prescription1 in 1 CARTONPASTE, DENTIFRICE13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83729-102SUPER MINT PRESCRIPTION (ANTICAVITY TOOTHPASTE) PASTE, DENTIFRICE [SUPERMOUTH, LLC.]2Current NDC, 2 package rows20241202_6773eb58-93b0-4e86-b780-7dde378c0bc3.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Super Mint PrescriptionANTICAVITY TOOTHPASTESuperMouth, LLC.6773eb58-93b0-4e86-b780-7dde378c0bc32025-11-12WarningsExact identifier
ndc (product): 83729-102

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
392038sodium fluoride 1.1 % ToothpastePSN6773eb58-93b0-4e86-b780-7dde378c0bc33
392038sodium fluoride 0.011 MG/MG ToothpasteSCD6773eb58-93b0-4e86-b780-7dde378c0bc33
392038sodium fluoride 1.1 % (fluoride ion 0.5 % ) ToothpasteSY6773eb58-93b0-4e86-b780-7dde378c0bc33
392038sodium fluoride 1.1 % Dental GelSY6773eb58-93b0-4e86-b780-7dde378c0bc33

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83729-102-10837290102101 TUBE in 1 CARTON (83729-102-10) / 96 g in 1 TUBE1 tube2023-10-13NoNoCurrent