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Up and Up Anticavity Toothpaste Whitening - 67659-082-02 - (Sodium Fluoride)

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Drug Information of Up and Up Anticavity Toothpaste Whitening

Product NDC: 67659-082
Proprietary Name: Up and Up Anticavity Toothpaste Whitening
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 Up and Up Anticavity Toothpaste Whitening

Product NDC: 67659-082
Labeler Name: Team Technologies, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100825

Package Information of Up and Up Anticavity Toothpaste Whitening

Package NDC: 67659-082-02
Package Description: 1 TUBE in 1 CARTON (67659-082-02) > 181.4 g in 1 TUBE (67659-082-01)

NDC Information of Up and Up Anticavity Toothpaste Whitening

NDC Code 67659-082-02
Proprietary Name Up and Up Anticavity Toothpaste Whitening
Package Description 1 TUBE in 1 CARTON (67659-082-02) > 181.4 g in 1 TUBE (67659-082-01)
Product NDC 67659-082
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Fluoride
Dosage Form Name PASTE, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20100825
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Team Technologies, Inc
Substance Name SODIUM FLUORIDE
Strength Number 2.43
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Up and Up Anticavity Toothpaste Whitening


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