| Product NDC: | 51117-001 |
| Proprietary Name: | Skincare LdeL Retinol |
| Non Proprietary Name: | Avobenzone, Homosalate, Oxybenzone, and Octinoxate |
| Active Ingredient(s): | 20; 30; 75; 50 mg/g; mg/g; mg/g; mg/g & nbsp; Avobenzone, Homosalate, Oxybenzone, and Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51117-001 |
| Labeler Name: | Beauty Solutions, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120905 |
| Package NDC: | 51117-001-01 |
| Package Description: | 1 JAR in 1 CARTON (51117-001-01) > 63 g in 1 JAR |
| NDC Code | 51117-001-01 |
| Proprietary Name | Skincare LdeL Retinol |
| Package Description | 1 JAR in 1 CARTON (51117-001-01) > 63 g in 1 JAR |
| Product NDC | 51117-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Oxybenzone, and Octinoxate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120905 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Beauty Solutions, Ltd. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OXYBENZONE |
| Strength Number | 20; 30; 75; 50 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |