EQUALINE - 41163-621-11 - (SELENIUM SULFIDE)

Alphabetical Index


Drug Information of EQUALINE

Product NDC: 41163-621
Proprietary Name: EQUALINE
Non Proprietary Name: SELENIUM SULFIDE
Active Ingredient(s): 10    mg/mL & nbsp;   SELENIUM SULFIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of EQUALINE

Product NDC: 41163-621
Labeler Name: SUPERVALU INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part358H
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130610

Package Information of EQUALINE

Package NDC: 41163-621-11
Package Description: 325 mL in 1 BOTTLE, PLASTIC (41163-621-11)

NDC Information of EQUALINE

NDC Code 41163-621-11
Proprietary Name EQUALINE
Package Description 325 mL in 1 BOTTLE, PLASTIC (41163-621-11)
Product NDC 41163-621
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SELENIUM SULFIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20130610
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name SUPERVALU INC.
Substance Name SELENIUM SULFIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of EQUALINE


General Information