Product NDC: | 50021-307 |
Proprietary Name: | SunZone Sunscreen Family SPF 30 |
Non Proprietary Name: | Octisalate, Oxybenzone, Avobenzone and Homosalate. |
Active Ingredient(s): | 3.02; 22.65; 7.55; 6.04 g/151g; g/151g; g/151g; g/151g & nbsp; Octisalate, Oxybenzone, Avobenzone and Homosalate. |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50021-307 |
Labeler Name: | Empack Spraytech Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121116 |
Package NDC: | 50021-307-01 |
Package Description: | 151 g in 1 CAN (50021-307-01) |
NDC Code | 50021-307-01 |
Proprietary Name | SunZone Sunscreen Family SPF 30 |
Package Description | 151 g in 1 CAN (50021-307-01) |
Product NDC | 50021-307 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octisalate, Oxybenzone, Avobenzone and Homosalate. |
Dosage Form Name | AEROSOL, SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20121116 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Empack Spraytech Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE |
Strength Number | 3.02; 22.65; 7.55; 6.04 |
Strength Unit | g/151g; g/151g; g/151g; g/151g |
Pharmaceutical Classes |