| 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: | 11410-405-42 |
| Package Description: | 1 TUBE in 1 BOX (11410-405-42) > 112 g in 1 TUBE (11410-405-41) |
| NDC Code | 11410-405-42 |
| Proprietary Name | Proactiv Solution Daily Protection Plus Sunscreen |
| Package Description | 1 TUBE in 1 BOX (11410-405-42) > 112 g in 1 TUBE (11410-405-41) |
| 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 |