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Advance White Extreme Whitening - 10237-658-72 - (Sodium Fluoride)

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Drug Information of Advance White Extreme Whitening

Product NDC: 10237-658
Proprietary Name: Advance White Extreme Whitening
Non Proprietary Name: Sodium Fluoride
Active Ingredient(s): 2.4    mg/g & nbsp;   Sodium Fluoride
Administration Route(s): DENTAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of Advance White Extreme Whitening

Product NDC: 10237-658
Labeler Name: Church & Dwight Co., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120129

Package Information of Advance White Extreme Whitening

Package NDC: 10237-658-72
Package Description: 1 TUBE in 1 CARTON (10237-658-72) > 204 g in 1 TUBE

NDC Information of Advance White Extreme Whitening

NDC Code 10237-658-72
Proprietary Name Advance White Extreme Whitening
Package Description 1 TUBE in 1 CARTON (10237-658-72) > 204 g in 1 TUBE
Product NDC 10237-658
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Fluoride
Dosage Form Name PASTE, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20120129
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Church & Dwight Co., Inc.
Substance Name SODIUM FLUORIDE
Strength Number 2.4
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Advance White Extreme Whitening


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