Product NDC: | 10812-199 |
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: | 10812-199 |
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: | 10812-199-01 |
Package Description: | 10 g in 1 TUBE (10812-199-01) |
NDC Code | 10812-199-01 |
Proprietary Name | Neutrogena MoistureShine Lip Soother |
Package Description | 10 g in 1 TUBE (10812-199-01) |
Product NDC | 10812-199 |
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 |