| Product NDC: | 10812-291 |
| Proprietary Name: | Neutrogena MoistureShine Lip Soother |
| Non Proprietary Name: | Octinoxate and Oxybenzone |
| Active Ingredient(s): | 75; 20 mg/g; mg/g & nbsp; Octinoxate and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10812-291 |
| Labeler Name: | Neutrogena Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130611 |
| Package NDC: | 10812-291-01 |
| Package Description: | 10 g in 1 TUBE (10812-291-01) |
| NDC Code | 10812-291-01 |
| Proprietary Name | Neutrogena MoistureShine Lip Soother |
| Package Description | 10 g in 1 TUBE (10812-291-01) |
| Product NDC | 10812-291 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Oxybenzone |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20130611 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neutrogena Corporation |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 75; 20 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |