Proactiv - 11410-603-28 - (OCTINOXATE and ZINC OXIDE)

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Drug Information of Proactiv

Product NDC: 11410-603
Proprietary Name: Proactiv
Non Proprietary Name: OCTINOXATE and ZINC OXIDE
Active Ingredient(s): 7.5; 3    mg/100mL; mg/100mL & nbsp;   OCTINOXATE and ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Proactiv

Product NDC: 11410-603
Labeler Name: Guthy-Renker LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20070101

Package Information of Proactiv

Package NDC: 11410-603-28
Package Description: 1 TUBE in 1 BOX (11410-603-28) > 75 mL in 1 TUBE

NDC Information of Proactiv

NDC Code 11410-603-28
Proprietary Name Proactiv
Package Description 1 TUBE in 1 BOX (11410-603-28) > 75 mL in 1 TUBE
Product NDC 11410-603
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE and ZINC OXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20070101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Guthy-Renker LLC
Substance Name OCTINOXATE; ZINC OXIDE
Strength Number 7.5; 3
Strength Unit mg/100mL; mg/100mL
Pharmaceutical Classes

Complete Information of Proactiv


General Information