Dandruff - 41190-311-15 - (Pyrithione zinc)

Alphabetical Index


Drug Information of Dandruff

Product NDC: 41190-311
Proprietary Name: Dandruff
Non Proprietary Name: Pyrithione zinc
Active Ingredient(s): 1    g/100mL & nbsp;   Pyrithione zinc
Administration Route(s): TOPICAL
Dosage Form(s): LOTION/SHAMPOO
Coding System: National Drug Codes(NDC)

Labeler Information of Dandruff

Product NDC: 41190-311
Labeler Name: Wakefern Food Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part358H
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090116

Package Information of Dandruff

Package NDC: 41190-311-15
Package Description: .42 mL in 1 BOTTLE, PLASTIC (41190-311-15)

NDC Information of Dandruff

NDC Code 41190-311-15
Proprietary Name Dandruff
Package Description .42 mL in 1 BOTTLE, PLASTIC (41190-311-15)
Product NDC 41190-311
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pyrithione zinc
Dosage Form Name LOTION/SHAMPOO
Route Name TOPICAL
Start Marketing Date 20090116
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Wakefern Food Corp
Substance Name PYRITHIONE ZINC
Strength Number 1
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Dandruff


General Information