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Crest Sensitivity - 37000-512-04 - (Potassium nitrate and Sodium Fluoride)

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Drug Information of Crest Sensitivity

Product NDC: 37000-512
Proprietary Name: Crest Sensitivity
Non Proprietary Name: Potassium nitrate and Sodium Fluoride
Active Ingredient(s): .05; 243    g/g; g/g & nbsp;   Potassium nitrate and Sodium Fluoride
Administration Route(s): DENTAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of Crest Sensitivity

Product NDC: 37000-512
Labeler Name: Procter & Gamble Manufacturing Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100830

Package Information of Crest Sensitivity

Package NDC: 37000-512-04
Package Description: 1 TUBE in 1 CARTON (37000-512-04) > 116 g in 1 TUBE

NDC Information of Crest Sensitivity

NDC Code 37000-512-04
Proprietary Name Crest Sensitivity
Package Description 1 TUBE in 1 CARTON (37000-512-04) > 116 g in 1 TUBE
Product NDC 37000-512
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Potassium nitrate and Sodium Fluoride
Dosage Form Name PASTE, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20100830
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Procter & Gamble Manufacturing Company
Substance Name POTASSIUM NITRATE; SODIUM FLUORIDE
Strength Number .05; 243
Strength Unit g/g; g/g
Pharmaceutical Classes

Complete Information of Crest Sensitivity


General Information