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Crest Cavity Protection - 37000-005-08 - (Sodium Fluoride)

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Drug Information of Crest Cavity Protection

Product NDC: 37000-005
Proprietary Name: Crest Cavity Protection
Non Proprietary Name: Sodium Fluoride
Active Ingredient(s): 2.43    mg/g & nbsp;   Sodium Fluoride
Administration Route(s): DENTAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of Crest Cavity Protection

Product NDC: 37000-005
Labeler Name: Procter & Gamble Manfuacturing Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19840802

Package Information of Crest Cavity Protection

Package NDC: 37000-005-08
Package Description: 1 TUBE in 1 CARTON (37000-005-08) > 24 g in 1 TUBE (37000-005-10)

NDC Information of Crest Cavity Protection

NDC Code 37000-005-08
Proprietary Name Crest Cavity Protection
Package Description 1 TUBE in 1 CARTON (37000-005-08) > 24 g in 1 TUBE (37000-005-10)
Product NDC 37000-005
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Fluoride
Dosage Form Name PASTE, DENTIFRICE
Route Name DENTAL
Start Marketing Date 19840802
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Procter & Gamble Manfuacturing Company
Substance Name SODIUM FLUORIDE
Strength Number 2.43
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Crest Cavity Protection


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