Super Mint

Manufacturer
SuperMouth, LLC.
Effective date
2025-07-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:06:35

Label at a glance#

ProductSuper Mint
Active ingredientSODIUM FLUORIDE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

DRUG FACTS

ACTIVE INGREDIENT

Sodium Fluoride 0.24% (0.15% w/v fluoride ion)

OTC - PURPOSE SECTION

PURPOSE
Anticavity Toothpaste

INDICATIONS & USAGE SECTION

USE

Aids in the prevention of cavities

WARNINGS SECTION

WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children under 6 years of age.

OTHER SAFETY INFORMATION

If more than used for brushing is accidentally swallowed, get medical help or
contact a Poison Control Center right away.

ALWAYS FOLLOW LABEL

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS

  • Children under 3 yrs: use no more than a tiny grain-of-rice smear.
  • Children between 3 and 6: use only a pea sized amount.

  • Place product on SuperMouth® toothbrush and brush teeth thoroughly at least
    twice a day for 2 minutes or use as directed by a Dentist or Physician. Supervise
    child’s brushing and rinsing to minimize swallowing.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS  Glycerin, Water, Hydrated Silica, *Hydroxamin®
(Nano-Hydroxyapatite, Menaquinone-7 (Vitamin K2), Cholecalciferol (Vitamin D3)),
Xylitol, Inulin, Natural Flavors, Sodium Gluconate, Methylsulfonylmethane, Xanthan
Gum, Quillaja Saponaria Extract, Sodium Methyl Cocoyl Taurate, Natural Benzoic
Acid, Sodium Ascorbate (Vitamin C), Stevia Leaf Extract, Cranberry Seed Oil.

Product Labeling: Super Mint Flouride Toothpaste

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

..........................................................................

Supermouth

super mint

fluoride toothpaste

safe • effective • fun

3.4 oz (96 g)

SuperMouth®

9737 Aero Drive,
San Diego, CA 92123
(844) MOUTHCARE

Super Mint -117Super Mint -117

res

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
416783sodium fluoride 0.24 % ToothpastePSN1
416783sodium fluoride 0.0024 MG/MG ToothpasteSCD1
416783sodium fluoride 0.24 % (fluoride ion 0.13 % ) ToothpasteSY1
416783sodium fluoride 0.24 % (fluoride ion 0.14 % ) ToothpasteSY1
416783sodium fluoride 0.24 % (fluoride ion 0.15 % ) ToothpasteSY1

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
83729-117-10Super Mint96 g in 1 TUBEPASTE, DENTIFRICE961
83729-117-10Super Mint1 in 1 CARTONPASTE, DENTIFRICE11

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83729-11783729-117-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

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 MintSUPER MINT TOOTHPASTESuperMouth, LLC.be0915f3-36c4-4200-9d15-704cfbd632b42025-07-05WarningsExact identifier
ndc (package): 83729-117-10
ndc (product): 83729-117
ndc11 (package): 83729011710
spl id: 6db22383-59b4-4da4-8016-8d1bedf9bc51
spl set id: be0915f3-36c4-4200-9d15-704cfbd632b4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.