MINTBLAST

Manufacturer
YOUNG PS ACQUISITION, LLC | Dabur India Limited
Effective date
2021-11-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:45:03

Label at a glance#

ProductMINTBLAST
Active ingredientSODIUM FLUORIDE
Label structure7 sections

Dosage and administration

Adults and children 2 years of age  and  older: Brush teeth thoroughly, preferably after each  meal or at least twice a day,  or use as directed by a dentist or a physician. Children  2 to  6  years: Use only a  pea sized amount and supervise child's brushing and rinsing  (to minimize swallowing) . Children under 2 year : Ask a dentist or physician .

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride -0.243 mg (0.15% w/v Fluoride ion)

Purpose

OTC - PURPOSE SECTION

Anticavity

Use

INDICATIONS & USAGE SECTION

Aids in the prevention of cavities.

Directions : 

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age  and  older: Brush teeth thoroughly, preferably after each  meal or at least twice a day,  or use as directed by a dentist or a physician.
  • Children  2 to  6  years: Use only a  pea sized amount and supervise child's brushing and rinsing  (to minimize swallowing) .
  • Children under 2 year : Ask a dentist or physician .

Warnings 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of  children under 6 years of age. If you accidentally swallow  more than used for brushing, seek professional assistance  or contact a Poison Control Center immediately.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

 Sorbitol, Silica , Treated Water , Poly Ethylene Glycol 1500 , Sodium Lauryl Sulfate , Flavor,  Titanium Dioxide , Cellulose Gum and/or Carrageenan, Tri Sodium Ortho Phosphate,   Saccharin Sodium, Tetra Sodium Pyrophosphate,Glycerine,  Color : FD&C Blue No.1

Mint Blast Product  Label 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
891775sodium fluoride 0.243 % ToothpastePSN3
891775sodium fluoride 0.00243 MG/MG ToothpasteSCD3
891775sodium fluoride 0.243 % (fluoride ion 0.13 % ) ToothpasteSY3
891775sodium fluoride 0.243 % (fluoride ion 0.14 % ) ToothpasteSY3
891775sodium fluoride 0.243 % (fluoride ion 0.15 % ) ToothpasteSY3
891775sodium fluoride 0.243 % (fluoride ion 0.16 % ) ToothpasteSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72326-8001-12025-01-30C16284748780-12cef2736-644c-d83d-e063-dadaa90ab31fMINTBLAST ANTICAVITY FLUORIDE TOOTH PASTE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72326-8001-1MINTBLAST28 g in 1 TUBEPASTE283

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72326-8001MINTBLAST (SODIUM FLUORIDE) PASTE [YOUNG PS ACQUISITION, LLC]3Legacy NDC, 1 package rows20211124_450821aa-e903-4a97-a152-8ea8ab5dd989.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72326-800172326-8001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
d174dd33-15a2-0f7c-e053-2995a90a9fee450821aa-e903-4a97-a152-8ea8ab5dd9892021-11-23Exact identifier
spl id: d174dd33-15a2-0f7c-e053-2995a90a9fee
spl set id: 450821aa-e903-4a97-a152-8ea8ab5dd989

Reported adverse events (FAERS/openFDA)#

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