Home
>
National Drug Code (NDC)
>
Proactiv
Proactiv - 11410-603-17 - (OCTINOXATE and ZINC OXIDE)
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: | 11410-603-17 |
| Package Description: | 1 TUBE in 1 BOX (11410-603-17) > 50 mL in 1 TUBE |
NDC Information of Proactiv
| NDC Code | 11410-603-17 |
| Proprietary Name | Proactiv |
| Package Description | 1 TUBE in 1 BOX (11410-603-17) > 50 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 |
