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 | |
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