NDC 51206-302

Opalescence Whitening

Sodium Fluoride

Opalescence 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 Sodium Fluoride.

Product ID51206-302_0421d6ee-000a-4658-9449-ec1a20c04a30
NDC51206-302
Product TypeHuman Otc Drug
Proprietary NameOpalescence Whitening
Generic NameSodium Fluoride
Dosage FormGel, Dentifrice
Route of AdministrationDENTAL
Marketing Start Date1994-07-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart355
Labeler NameUltradent Products, Inc.
Substance NameSODIUM FLUORIDE
Active Ingredient Strength1 mg/g
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 51206-302-06

1 TUBE in 1 BOX (51206-302-06) > 133 g in 1 TUBE
Marketing Start Date1994-07-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51206-302-08 [51206030208]

Opalescence Whitening GEL, DENTIFRICE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-01

NDC 51206-302-09 [51206030209]

Opalescence Whitening GEL, DENTIFRICE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-01

NDC 51206-302-10 [51206030210]

Opalescence Whitening GEL, DENTIFRICE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-01

NDC 51206-302-07 [51206030207]

Opalescence Whitening GEL, DENTIFRICE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date1994-07-01

NDC 51206-302-06 [51206030206]

Opalescence Whitening GEL, DENTIFRICE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date1994-07-01

Drug Details

Active Ingredients

IngredientStrength
SODIUM FLUORIDE1.1 mg/g

OpenFDA Data

SPL SET ID:d07f842e-b6f1-4ae1-b576-f542ecd02dd4
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1044547

    • NDC Crossover Matching brand name "Opalescence Whitening" or generic name "Sodium Fluoride"

    NDCBrand NameGeneric Name
    51206-302Opalescence WhiteningOpalescence Whitening
    0135-0234AQUAFRESHsodium fluoride
    0126-0021ColgateSODIUM FLUORIDE
    0126-0034Colgate Phos-Flur Ortho Defense Alcohol Free Anticavity Gushing Grape FluorideSODIUM FLUORIDE
    0126-0032Colgate Phos-Flur Ortho Defense Alcohol Free Anticavity Mint FluorideSODIUM FLUORIDE
    0041-1421Oral-BSodium Fluoride
    0126-0131Phos-FlurSodium Fluoride
    0126-0135Phos-Flur Ortho DefenseSODIUM FLUORIDE
    0126-0138Phos-Flur Ortho DefenseSODIUM FLUORIDE
    0126-0139Phos-Flur Ortho DefenseSODIUM FLUORIDE
    0126-0074PrevidDent 5000 Booster Plus SpearmintSodium Fluoride
    0126-0016PreviDentSodium fluoride
    0126-0075PreviDentSodium fluoride
    0126-0076PreviDentSodium fluoride
    0126-0179PreviDentSodium Fluoride
    0126-0286PreviDentSodium Fluoride
    0126-0287PreviDentSodium Fluoride
    0126-0072PreviDent 5000 Booster Plus FruitasticSodium Fluoride
    0126-0033PreviDent Alcohol FreeSodium Fluoride
    0126-0088PreviDent Fresh MintSodium Fluoride
    0126-0289PreviDent OrthoDefenseSODIUM FLUORIDE
    0126-0288PreviDent Very BerrySodium Fluoride
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