Product NDC: | 11410-001 |
Proprietary Name: | Proactiv Solution BB Broad Spectrum SPF 15 (Light, Medium, Dark) |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, and OXYBENZONE |
Active Ingredient(s): | 7.5; 5; 3 g/100mL; mg/100mL; mg/100mL & nbsp; OCTINOXATE, OCTISALATE, and OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11410-001 |
Labeler Name: | Guthy-Renker LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121201 |
Package NDC: | 11410-001-17 |
Package Description: | 1 TUBE in 1 BOX (11410-001-17) > 50 mL in 1 TUBE |
NDC Code | 11410-001-17 |
Proprietary Name | Proactiv Solution BB Broad Spectrum SPF 15 (Light, Medium, Dark) |
Package Description | 1 TUBE in 1 BOX (11410-001-17) > 50 mL in 1 TUBE |
Product NDC | 11410-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, and OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20121201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Guthy-Renker LLC |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 7.5; 5; 3 |
Strength Unit | g/100mL; mg/100mL; mg/100mL |
Pharmaceutical Classes |