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Proactiv Solution - 11410-601-41 - (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OXYBENZONE)

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Drug Information of Proactiv Solution

Product NDC: 11410-601
Proprietary Name: Proactiv Solution
Non Proprietary Name: AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OXYBENZONE
Active Ingredient(s): 2; 5; 7.5; 5; 5    mg/100g; mL/100g; mL/100g; mL/100g; mg/100g & nbsp;   AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Proactiv Solution

Product NDC: 11410-601
Labeler Name: Guthy-Renker LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110607

Package Information of Proactiv Solution

Package NDC: 11410-601-41
Package Description: 112 g in 1 TUBE (11410-601-41)

NDC Information of Proactiv Solution

NDC Code 11410-601-41
Proprietary Name Proactiv Solution
Package Description 112 g in 1 TUBE (11410-601-41)
Product NDC 11410-601
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OXYBENZONE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110607
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Guthy-Renker LLC.
Substance Name AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 2; 5; 7.5; 5; 5
Strength Unit mg/100g; mL/100g; mL/100g; mL/100g; mg/100g
Pharmaceutical Classes

Complete Information of Proactiv Solution


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