NDC 51206-308

Opalescence Sensitivity Relief Whitening

Potassium Nitrate And Sodium Fluoride

Opalescence Sensitivity Relief Whitening is a Dental Gel, Dentifrice in the Human Otc Drug category. It is labeled and distributed by Ultradent Products, Inc.. The primary component is Potassium Nitrate; Sodium Fluoride.

Product ID51206-308_3459eab1-718a-4fad-ad1c-ce3c7a9ad93b
NDC51206-308
Product TypeHuman Otc Drug
Proprietary NameOpalescence Sensitivity Relief Whitening
Generic NamePotassium Nitrate And Sodium Fluoride
Dosage FormGel, Dentifrice
Route of AdministrationDENTAL
Marketing Start Date2015-11-30
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart356
Labeler NameUltradent Products, Inc.
Substance NamePOTASSIUM NITRATE; SODIUM FLUORIDE
Active Ingredient Strength50 mg/g; mg/g
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 51206-308-01

1 TUBE in 1 CARTON (51206-308-01) > 28.35 g in 1 TUBE
Marketing Start Date2015-11-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51206-308-05 [51206030805]

Opalescence Sensitivity Relief Whitening GEL, DENTIFRICE
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-30

NDC 51206-308-01 [51206030801]

Opalescence Sensitivity Relief Whitening GEL, DENTIFRICE
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-30

NDC 51206-308-04 [51206030804]

Opalescence Sensitivity Relief Whitening GEL, DENTIFRICE
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-30

NDC 51206-308-03 [51206030803]

Opalescence Sensitivity Relief Whitening GEL, DENTIFRICE
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-30

NDC 51206-308-02 [51206030802]

Opalescence Sensitivity Relief Whitening GEL, DENTIFRICE
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-30

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM NITRATE50 mg/g

OpenFDA Data

SPL SET ID:b5176a84-76a3-4ad0-a2e2-4997a12da9a5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1086243

    • NDC Crossover Matching brand name "Opalescence Sensitivity Relief Whitening" or generic name "Potassium Nitrate And Sodium Fluoride"

    NDCBrand NameGeneric Name
    51206-308Opalescence Sensitivity Relief WhiteningOpalescence Sensitivity Relief Whitening
    0135-0525Sensodynepotassium nitrate and sodium fluoride
    0135-0526Sensodynepotassium nitrate and sodium fluoride
    0135-0527Sensodynepotassium nitrate and sodium fluoride
    0135-0528Sensodynepotassium nitrate and sodium fluoride
    0135-0450SENSODYNE PRONAMELpotassium nitrate and sodium fluoride
    0135-0460SENSODYNE PRONAMELpotassium nitrate and sodium fluoride
    0135-0480SENSODYNE PRONAMELpotassium nitrate and sodium fluoride
    0135-0481SENSODYNE PRONAMELpotassium nitrate and sodium fluoride
    0135-0484SENSODYNE PRONAMELpotassium nitrate and sodium fluoride
    0135-0486SENSODYNE PRONAMELpotassium nitrate and sodium fluoride
    0135-0492SENSODYNE PRONAMELpotassium nitrate and sodium fluoride
    0135-0520SENSODYNE PRONAMELpotassium nitrate and sodium fluoride
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