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OBAGI C RX SYSTEM C CLARIFYING SERUM
OBAGI C RX SYSTEM C CLARIFYING SERUM - 62032-122-10 - (HYDROQUINONE)
Drug Information of OBAGI C RX SYSTEM C CLARIFYING SERUM
| Product NDC: | 62032-122 |
| Proprietary Name: | OBAGI C RX SYSTEM C CLARIFYING SERUM |
| Non Proprietary Name: | HYDROQUINONE |
| Active Ingredient(s): | 40 mg/mL & nbsp; HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OBAGI C RX SYSTEM C CLARIFYING SERUM
| Product NDC: | 62032-122 |
| Labeler Name: | OMP, INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100101 |
Package Information of OBAGI C RX SYSTEM C CLARIFYING SERUM
| Package NDC: | 62032-122-10 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (62032-122-10) > 30 mL in 1 BOTTLE, GLASS |
NDC Information of OBAGI C RX SYSTEM C CLARIFYING SERUM
| NDC Code | 62032-122-10 |
| Proprietary Name | OBAGI C RX SYSTEM C CLARIFYING SERUM |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (62032-122-10) > 30 mL in 1 BOTTLE, GLASS |
| Product NDC | 62032-122 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | OMP, INC. |
| Substance Name | HYDROQUINONE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA] |
