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Hydroquinone
Hydroquinone - 68788-9916-2 - (HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O)
Drug Information of Hydroquinone
| Product NDC: | 68788-9916 |
| Proprietary Name: | Hydroquinone |
| Non Proprietary Name: | HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O |
| Active Ingredient(s): | 30; 40; 20; 80 mg/g; mg/g; mg/g; mg/g & nbsp; HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydroquinone
| Product NDC: | 68788-9916 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120130 |
Package Information of Hydroquinone
| Package NDC: | 68788-9916-2 |
| Package Description: | 1 TUBE in 1 CARTON (68788-9916-2) > 28.35 g in 1 TUBE |
NDC Information of Hydroquinone
| NDC Code | 68788-9916-2 |
| Proprietary Name | Hydroquinone |
| Package Description | 1 TUBE in 1 CARTON (68788-9916-2) > 28.35 g in 1 TUBE |
| Product NDC | 68788-9916 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120130 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | DIOXYBENZONE; HYDROQUINONE; OXYBENZONE; PADIMATE O |
| Strength Number | 30; 40; 20; 80 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes | Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA] |
