Product NDC: | 66273-0004 |
Proprietary Name: | CLEAR ACTION |
Non Proprietary Name: | HYDROQUINONE |
Active Ingredient(s): | 10 mL/500mL & nbsp; HYDROQUINONE |
Administration Route(s): | CUTANEOUS |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66273-0004 |
Labeler Name: | AQUIMPEX SPA |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part358A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110719 |
Package NDC: | 66273-0004-3 |
Package Description: | 12 CELLO PACK in 1 BOX (66273-0004-3) > 1 BOTTLE, PLASTIC in 1 CELLO PACK (66273-0004-2) > 500 mL in 1 BOTTLE, PLASTIC (66273-0004-1) |
NDC Code | 66273-0004-3 |
Proprietary Name | CLEAR ACTION |
Package Description | 12 CELLO PACK in 1 BOX (66273-0004-3) > 1 BOTTLE, PLASTIC in 1 CELLO PACK (66273-0004-2) > 500 mL in 1 BOTTLE, PLASTIC (66273-0004-1) |
Product NDC | 66273-0004 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HYDROQUINONE |
Dosage Form Name | LOTION |
Route Name | CUTANEOUS |
Start Marketing Date | 20110719 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AQUIMPEX SPA |
Substance Name | HYDROQUINONE |
Strength Number | 10 |
Strength Unit | mL/500mL |
Pharmaceutical Classes |