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Equaline Dandruff - 41163-423-14 - (PYRITHIONE ZINC)

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Drug Information of Equaline Dandruff

Product NDC: 41163-423
Proprietary Name: Equaline Dandruff
Non Proprietary Name: PYRITHIONE ZINC
Active Ingredient(s): 1    mL/100mL & nbsp;   PYRITHIONE ZINC
Administration Route(s): TOPICAL
Dosage Form(s): SHAMPOO
Coding System: National Drug Codes(NDC)

Labeler Information of Equaline Dandruff

Product NDC: 41163-423
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part358H
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100916

Package Information of Equaline Dandruff

Package NDC: 41163-423-14
Package Description: 420 mL in 1 BOTTLE, PLASTIC (41163-423-14)

NDC Information of Equaline Dandruff

NDC Code 41163-423-14
Proprietary Name Equaline Dandruff
Package Description 420 mL in 1 BOTTLE, PLASTIC (41163-423-14)
Product NDC 41163-423
Product Type Name HUMAN OTC DRUG
Non Proprietary Name PYRITHIONE ZINC
Dosage Form Name SHAMPOO
Route Name TOPICAL
Start Marketing Date 20100916
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Supervalu Inc
Substance Name PYRITHIONE ZINC
Strength Number 1
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Equaline Dandruff


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