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Rembrandt Deeply White Plus Peroxide Whitening - 42002-616-01 - (Sodium Monofluorophosphate)

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Drug Information of Rembrandt Deeply White Plus Peroxide Whitening

Product NDC: 42002-616
Proprietary Name: Rembrandt Deeply White Plus Peroxide Whitening
Non Proprietary Name: Sodium Monofluorophosphate
Active Ingredient(s): 1.5    mg/g & nbsp;   Sodium Monofluorophosphate
Administration Route(s): ORAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of Rembrandt Deeply White Plus Peroxide Whitening

Product NDC: 42002-616
Labeler Name: Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120316

Package Information of Rembrandt Deeply White Plus Peroxide Whitening

Package NDC: 42002-616-01
Package Description: 1 TUBE in 1 CARTON (42002-616-01) > 74 g in 1 TUBE

NDC Information of Rembrandt Deeply White Plus Peroxide Whitening

NDC Code 42002-616-01
Proprietary Name Rembrandt Deeply White Plus Peroxide Whitening
Package Description 1 TUBE in 1 CARTON (42002-616-01) > 74 g in 1 TUBE
Product NDC 42002-616
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Monofluorophosphate
Dosage Form Name PASTE, DENTIFRICE
Route Name ORAL
Start Marketing Date 20120316
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
Substance Name SODIUM MONOFLUOROPHOSPHATE
Strength Number 1.5
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Rembrandt Deeply White Plus Peroxide Whitening


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