Proactiv - 11410-812-29 - (SULFUR)

Alphabetical Index


Drug Information of Proactiv

Product NDC: 11410-812
Proprietary Name: Proactiv
Non Proprietary Name: SULFUR
Active Ingredient(s): 6    mg/100mL & nbsp;   SULFUR
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Proactiv

Product NDC: 11410-812
Labeler Name: Guthy-Renker LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080201

Package Information of Proactiv

Package NDC: 11410-812-29
Package Description: 1 TUBE in 1 BOX (11410-812-29) > 30 mL in 1 TUBE

NDC Information of Proactiv

NDC Code 11410-812-29
Proprietary Name Proactiv
Package Description 1 TUBE in 1 BOX (11410-812-29) > 30 mL in 1 TUBE
Product NDC 11410-812
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SULFUR
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20080201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Guthy-Renker LLC
Substance Name SULFUR
Strength Number 6
Strength Unit mg/100mL
Pharmaceutical Classes

Complete Information of Proactiv


General Information