Genesis Sensitive Fresh Mint

Manufacturer
Dr Bobs Inc
Effective date
2017-09-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:11:46

Label at a glance#

ProductGenesis Sensitive Fresh Mint
Active ingredientPOTASSIUM NITRATE, SODIUM FLUORIDE
Label structure8 sections

Indications and uses

builds increasing protection against painful sensitivity of the teeth due to cold, heat, acids, sweets or contact aids in the prevention of dental cavities

Dosage and administration

adults and children 12 years of age and older  apply at least a 1-inch strip of product onto a soft bristle toothbrush  brush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by a dentist or doctor.  Make sure to brush all sensitive areas of the teeth.  Minimize swallowing, Spit out after brushing children under 12 years of age: consult a ...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Potassium nitrate 5%

Sodium fluoride (0.15% w/v fluoride ion)

Purpose

OTC - PURPOSE SECTION

Antihypersensitivity

Anticavity

Uses

INDICATIONS & USAGE SECTION

  • builds increasing protection against painful sensitivity of the teeth due to cold, heat, acids, sweets or contact
  • aids in the prevention of dental cavities

Warnings

WARNINGS SECTION

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • the problem persists or worsens, Sensitive teeth may indicate a serious problem that may prompt care by a dentist
  • pain sensitivity still persist after 4 weeks of use 

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years of age and older 
  • apply at least a 1-inch strip of product onto a soft bristle toothbrush 
  • brush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by a dentist or doctor.  Make sure to brush all sensitive areas of the teeth.  Minimize swallowing, Spit out after brushing
  • children under 12 years of age: consult a dentist or doctor

Other information

SPL UNCLASSIFIED SECTION

  • store below 30°C (86°F)
  • Lot No. & Exp Date: see box or see crimp of tube

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Silica, Sorbitol, Sodium Lauryl Alcohol, Polyethylene Glycol 300, Sodium Carboxymethylcellulose, Flavor, Sodium Saccharin, Titanium Dioxide, Sodium Pyrophosphate, Sodium Hydroxide, PEG/PPG115/55 copolymer, Color FD&C Blue #1

​Questions or comments?

OTC - QUESTIONS SECTION

Contact customerservice@genesisbrush.com

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Package

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71771-001-002020-02-03C16284748780-19d75b9d0-33be-f424-e053-dadaa90a57ceGenesis Sensitive Toothpaste Fresh Mint
71771-001-002020-01-31C16284748780-19d75b9d0-33be-f424-e053-dadaa90a57ceGenesis Sensitive Toothpaste Fresh Mint

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71771-00171771-001-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
5a41534d-e77e-e4ac-e053-2a91aa0afa8ae72979ac-b7d0-49a6-ab5d-3248621a9ad92017-09-28WarningsExact identifier
spl id: 5a41534d-e77e-e4ac-e053-2a91aa0afa8a
spl set id: e72979ac-b7d0-49a6-ab5d-3248621a9ad9

Reported adverse events (FAERS/openFDA)#

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