Product NDC: | 51830-019 |
Proprietary Name: | Lightening Day Cream |
Non Proprietary Name: | DICAPRYLYL CARBONATE |
Active Ingredient(s): | 2.5 mg/50mg & nbsp; DICAPRYLYL CARBONATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51830-019 |
Labeler Name: | LANGE SAS |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120718 |
Package NDC: | 51830-019-04 |
Package Description: | 50 mg in 1 CONTAINER (51830-019-04) |
NDC Code | 51830-019-04 |
Proprietary Name | Lightening Day Cream |
Package Description | 50 mg in 1 CONTAINER (51830-019-04) |
Product NDC | 51830-019 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DICAPRYLYL CARBONATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120718 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | LANGE SAS |
Substance Name | POLYETHYLENE GLYCOL 400 |
Strength Number | 2.5 |
Strength Unit | mg/50mg |
Pharmaceutical Classes |