Product NDC: | 50021-243 |
Proprietary Name: | SunZone Family Sunscreen SPF-60 |
Non Proprietary Name: | Avobenzone and Octinoxate |
Active Ingredient(s): | 7.02; 9.36 g/234g; g/234g & nbsp; Avobenzone and Octinoxate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50021-243 |
Labeler Name: | Empack Spraytech Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121113 |
Package NDC: | 50021-243-01 |
Package Description: | 234 g in 1 TUBE (50021-243-01) |
NDC Code | 50021-243-01 |
Proprietary Name | SunZone Family Sunscreen SPF-60 |
Package Description | 234 g in 1 TUBE (50021-243-01) |
Product NDC | 50021-243 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone and Octinoxate |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20121113 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Empack Spraytech Inc. |
Substance Name | AVOBENZONE; OCTINOXATE |
Strength Number | 7.02; 9.36 |
Strength Unit | g/234g; g/234g |
Pharmaceutical Classes |