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Lightening Day Cream
Lightening Day Cream - 51830-019-04 - (DICAPRYLYL CARBONATE)
Drug Information of Lightening Day Cream
| 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) |
Labeler Information of Lightening Day Cream
| 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 Information of Lightening Day Cream
| Package NDC: | 51830-019-04 |
| Package Description: | 50 mg in 1 CONTAINER (51830-019-04) |
NDC Information of Lightening Day Cream
| 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 |
