Product NDC: | 10812-968 |
Proprietary Name: | Neutrogena Wet Skin Swim-Humidity-Sweat Sunscreen |
Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
Active Ingredient(s): | 30; 80; 40; 80; 50 mg/g; mg/g; mg/g; mg/g; mg/g & nbsp; AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10812-968 |
Labeler Name: | Neutrogena Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101201 |
Package NDC: | 10812-968-01 |
Package Description: | 141 g in 1 CAN (10812-968-01) |
NDC Code | 10812-968-01 |
Proprietary Name | Neutrogena Wet Skin Swim-Humidity-Sweat Sunscreen |
Package Description | 141 g in 1 CAN (10812-968-01) |
Product NDC | 10812-968 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
Dosage Form Name | AEROSOL, SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20101201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Neutrogena Corporation |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 30; 80; 40; 80; 50 |
Strength Unit | mg/g; mg/g; mg/g; mg/g; mg/g |
Pharmaceutical Classes |