Product NDC: | 66273-0002 |
Proprietary Name: | EXENCE WHITE |
Non Proprietary Name: | HYDROQUINONE |
Active Ingredient(s): | 4 mL/200mL & nbsp; HYDROQUINONE |
Administration Route(s): | CUTANEOUS |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66273-0002 |
Labeler Name: | AQUIMPEX SPA |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part358A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110712 |
Package NDC: | 66273-0002-2 |
Package Description: | 12 BOTTLE, PLASTIC in 1 BOX (66273-0002-2) > 500 mL in 1 BOTTLE, PLASTIC (66273-0002-1) |
NDC Code | 66273-0002-2 |
Proprietary Name | EXENCE WHITE |
Package Description | 12 BOTTLE, PLASTIC in 1 BOX (66273-0002-2) > 500 mL in 1 BOTTLE, PLASTIC (66273-0002-1) |
Product NDC | 66273-0002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HYDROQUINONE |
Dosage Form Name | LOTION |
Route Name | CUTANEOUS |
Start Marketing Date | 20110712 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AQUIMPEX SPA |
Substance Name | HYDROQUINONE |
Strength Number | 4 |
Strength Unit | mL/200mL |
Pharmaceutical Classes |