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NU-DERM SUNFADER
NU-DERM SUNFADER - 62032-116-36 - (HYDROQUINONE, OCTINOXATE, and OXYBENZONE)
Drug Information of NU-DERM SUNFADER
| Product NDC: | 62032-116 |
| Proprietary Name: | NU-DERM SUNFADER |
| Non Proprietary Name: | HYDROQUINONE, OCTINOXATE, and OXYBENZONE |
| Active Ingredient(s): | 40; 75; 55 mg/g; mg/g; mg/g & nbsp; HYDROQUINONE, OCTINOXATE, and OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NU-DERM SUNFADER
| Product NDC: | 62032-116 |
| Labeler Name: | OMP, INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19840101 |
Package Information of NU-DERM SUNFADER
| Package NDC: | 62032-116-36 |
| Package Description: | 57 g in 1 BOTTLE, PLASTIC (62032-116-36) |
NDC Information of NU-DERM SUNFADER
| NDC Code | 62032-116-36 |
| Proprietary Name | NU-DERM SUNFADER |
| Package Description | 57 g in 1 BOTTLE, PLASTIC (62032-116-36) |
| Product NDC | 62032-116 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROQUINONE, OCTINOXATE, and OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19840101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | OMP, INC. |
| Substance Name | HYDROQUINONE; OCTINOXATE; OXYBENZONE |
| Strength Number | 40; 75; 55 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes | Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA] |
