Dandruff - 55910-311-35 - (Pyrithione zinc)

Alphabetical Index


Drug Information of Dandruff

Product NDC: 55910-311
Proprietary Name: Dandruff
Non Proprietary Name: Pyrithione zinc
Active Ingredient(s): 1    kg/100L & nbsp;   Pyrithione zinc
Administration Route(s): TOPICAL
Dosage Form(s): SHAMPOO
Coding System: National Drug Codes(NDC)

Labeler Information of Dandruff

Product NDC: 55910-311
Labeler Name: Dolgencorp, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part358H
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20050623

Package Information of Dandruff

Package NDC: 55910-311-35
Package Description: .701 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55910-311-35) > .42 L in 1 BOTTLE, PLASTIC (55910-311-15)

NDC Information of Dandruff

NDC Code 55910-311-35
Proprietary Name Dandruff
Package Description .701 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55910-311-35) > .42 L in 1 BOTTLE, PLASTIC (55910-311-15)
Product NDC 55910-311
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pyrithione zinc
Dosage Form Name SHAMPOO
Route Name TOPICAL
Start Marketing Date 20050623
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Dolgencorp, LLC
Substance Name PYRITHIONE ZINC
Strength Number 1
Strength Unit kg/100L
Pharmaceutical Classes

Complete Information of Dandruff


General Information