Home
>
National Drug Code (NDC)
>
AGELESS Total Skin Bleaching Serum
AGELESS Total Skin Bleaching Serum - 62742-4033-1 - (HYDROQUINONE)
Drug Information of AGELESS Total Skin Bleaching Serum
| Product NDC: | 62742-4033 |
| Proprietary Name: | AGELESS Total Skin Bleaching Serum |
| Non Proprietary Name: | HYDROQUINONE |
| Active Ingredient(s): | 20 mg/mL & nbsp; HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AGELESS Total Skin Bleaching Serum
| Product NDC: | 62742-4033 |
| Labeler Name: | Allure Labs, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100101 |
Package Information of AGELESS Total Skin Bleaching Serum
| Package NDC: | 62742-4033-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (62742-4033-1) |
NDC Information of AGELESS Total Skin Bleaching Serum
| NDC Code | 62742-4033-1 |
| Proprietary Name | AGELESS Total Skin Bleaching Serum |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (62742-4033-1) |
| Product NDC | 62742-4033 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Allure Labs, Inc. |
| Substance Name | HYDROQUINONE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
