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Neutrogena MoistureShine SPF20
Neutrogena MoistureShine SPF20 - 10812-341-01 - (Octinoxate, Octisalate, and Titanium Dioxide)
Drug Information of Neutrogena MoistureShine SPF20
| Product NDC: | 10812-341 |
| Proprietary Name: | Neutrogena MoistureShine SPF20 |
| Non Proprietary Name: | Octinoxate, Octisalate, and Titanium Dioxide |
| Active Ingredient(s): | 50; 25; 11 mg/g; mg/g; mg/g & nbsp; Octinoxate, Octisalate, and Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neutrogena MoistureShine SPF20
| Product NDC: | 10812-341 |
| Labeler Name: | Neutrogena Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100215 |
Package Information of Neutrogena MoistureShine SPF20
| Package NDC: | 10812-341-01 |
| Package Description: | 3.4 g in 1 TUBE (10812-341-01) |
NDC Information of Neutrogena MoistureShine SPF20
| NDC Code | 10812-341-01 |
| Proprietary Name | Neutrogena MoistureShine SPF20 |
| Package Description | 3.4 g in 1 TUBE (10812-341-01) |
| Product NDC | 10812-341 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, and Titanium Dioxide |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20100215 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Neutrogena Corporation |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Strength Number | 50; 25; 11 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
