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Listerine Whitening Restoring - 42002-420-16 - (Sodium Fluoride)

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Drug Information of Listerine Whitening Restoring

Product NDC: 42002-420
Proprietary Name: Listerine Whitening Restoring
Non Proprietary Name: Sodium Fluoride
Active Ingredient(s): .2    mg/mL & nbsp;   Sodium Fluoride
Administration Route(s): ORAL
Dosage Form(s): RINSE
Coding System: National Drug Codes(NDC)

Labeler Information of Listerine Whitening Restoring

Product NDC: 42002-420
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: 20120501

Package Information of Listerine Whitening Restoring

Package NDC: 42002-420-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC (42002-420-16)

NDC Information of Listerine Whitening Restoring

NDC Code 42002-420-16
Proprietary Name Listerine Whitening Restoring
Package Description 473 mL in 1 BOTTLE, PLASTIC (42002-420-16)
Product NDC 42002-420
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Fluoride
Dosage Form Name RINSE
Route Name ORAL
Start Marketing Date 20120501
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
Substance Name SODIUM FLUORIDE
Strength Number .2
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Listerine Whitening Restoring


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