| Product NDC: | 62032-509 |
| Proprietary Name: | CONDITION AND ENHANCE SYSTEM |
| Non Proprietary Name: | HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |
| Active Ingredient(s): | & nbsp; HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62032-509 |
| Labeler Name: | OMP, INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20070820 |
| Package NDC: | 62032-509-01 |
| Package Description: | 1 KIT in 1 CARTON (62032-509-01) * 90 mL in 1 BOTTLE, PLASTIC (62032-119-90) * 200 mL in 1 BOTTLE, PLASTIC * 200 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-117-36) * 57 g in 1 BOTTLE, PLASTIC (62032-115-36) |
| NDC Code | 62032-509-01 |
| Proprietary Name | CONDITION AND ENHANCE SYSTEM |
| Package Description | 1 KIT in 1 CARTON (62032-509-01) * 90 mL in 1 BOTTLE, PLASTIC (62032-119-90) * 200 mL in 1 BOTTLE, PLASTIC * 200 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-117-36) * 57 g in 1 BOTTLE, PLASTIC (62032-115-36) |
| Product NDC | 62032-509 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20070820 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | OMP, INC. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |