Product NDC: | 50021-152 |
Proprietary Name: | SunZone Family SPF 45 |
Non Proprietary Name: | Octocrylene, Octisalate, Homosalate, Avobenzone and Oxybenzone |
Active Ingredient(s): | 3; 15; 7.5; 3; 7.5 g/150g; g/150g; g/150g; g/150g; g/150g & nbsp; Octocrylene, Octisalate, Homosalate, Avobenzone and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50021-152 |
Labeler Name: | Empack Spraytech Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121119 |
Package NDC: | 50021-152-01 |
Package Description: | 150 g in 1 CAN (50021-152-01) |
NDC Code | 50021-152-01 |
Proprietary Name | SunZone Family SPF 45 |
Package Description | 150 g in 1 CAN (50021-152-01) |
Product NDC | 50021-152 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octocrylene, Octisalate, Homosalate, Avobenzone and Oxybenzone |
Dosage Form Name | AEROSOL, SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20121119 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Empack Spraytech Inc |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 3; 15; 7.5; 3; 7.5 |
Strength Unit | g/150g; g/150g; g/150g; g/150g; g/150g |
Pharmaceutical Classes |