Product NDC: | 11410-405 |
Proprietary Name: | Proactiv Solution Daily Protection Plus Sunscreen |
Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OXYBENZONE |
Active Ingredient(s): | 2; 5; 7.5; 5; 5 mg/.1g; mg/.1g; mL/.1g; mg/.1g; mg/.1g & nbsp; AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11410-405 |
Labeler Name: | Guthy-Renker LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20040101 |
Package NDC: | 11410-405-17 |
Package Description: | 48 g in 1 TUBE (11410-405-17) |
NDC Code | 11410-405-17 |
Proprietary Name | Proactiv Solution Daily Protection Plus Sunscreen |
Package Description | 48 g in 1 TUBE (11410-405-17) |
Product NDC | 11410-405 |
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 | 20040101 |
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/.1g; mg/.1g; mL/.1g; mg/.1g; mg/.1g |
Pharmaceutical Classes |