Product NDC: | 10812-418 |
Proprietary Name: | Neutrogena Beach Defense Water Plus Sun Barrier |
Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
Active Ingredient(s): | 27; 80; 50; 35; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10812-418 |
Labeler Name: | Neutrogena Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120601 |
Package NDC: | 10812-418-01 |
Package Description: | 198 mL in 1 BOTTLE, PUMP (10812-418-01) |
NDC Code | 10812-418-01 |
Proprietary Name | Neutrogena Beach Defense Water Plus Sun Barrier |
Package Description | 198 mL in 1 BOTTLE, PUMP (10812-418-01) |
Product NDC | 10812-418 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120601 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Neutrogena Corporation |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 27; 80; 50; 35; 40 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |