Product NDC: | 49520-201 |
Proprietary Name: | LIGHT THE WAY |
Non Proprietary Name: | HYDROQUINONE |
Active Ingredient(s): | 2 g/100mL & nbsp; HYDROQUINONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49520-201 |
Labeler Name: | mybody |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part358A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120424 |
Package NDC: | 49520-201-51 |
Package Description: | 1 BOTTLE in 1 BOX (49520-201-51) > 15 mL in 1 BOTTLE (49520-201-11) |
NDC Code | 49520-201-51 |
Proprietary Name | LIGHT THE WAY |
Package Description | 1 BOTTLE in 1 BOX (49520-201-51) > 15 mL in 1 BOTTLE (49520-201-11) |
Product NDC | 49520-201 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HYDROQUINONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120424 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | mybody |
Substance Name | HYDROQUINONE |
Strength Number | 2 |
Strength Unit | g/100mL |
Pharmaceutical Classes |