Product NDC: | 50021-235 |
Proprietary Name: | SunZone Family SPF 30 |
Non Proprietary Name: | Octinoxate and Avobenzone |
Active Ingredient(s): | 1.76; 4.7 g/235g; g/235g & nbsp; Octinoxate and Avobenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50021-235 |
Labeler Name: | Empack Spraytech Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121112 |
Package NDC: | 50021-235-03 |
Package Description: | 235 g in 1 TUBE (50021-235-03) |
NDC Code | 50021-235-03 |
Proprietary Name | SunZone Family SPF 30 |
Package Description | 235 g in 1 TUBE (50021-235-03) |
Product NDC | 50021-235 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate and Avobenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20121112 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Empack Spraytech Inc |
Substance Name | AVOBENZONE; OCTINOXATE |
Strength Number | 1.76; 4.7 |
Strength Unit | g/235g; g/235g |
Pharmaceutical Classes |