Home
>
National Drug Code (NDC)
>
Sunzone Family SPF 15
Sunzone Family SPF 15 - 50021-016-01 - (Octinoxate and Avobenzone)
Drug Information of Sunzone Family SPF 15
| Product NDC: | 50021-016 |
| Proprietary Name: | Sunzone Family SPF 15 |
| Non Proprietary Name: | Octinoxate and Avobenzone |
| Active Ingredient(s): | 1.18; 2.35 g/235g; g/235g & nbsp; Octinoxate and Avobenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunzone Family SPF 15
| Product NDC: | 50021-016 |
| Labeler Name: | Empack Spraytech Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121114 |
Package Information of Sunzone Family SPF 15
| Package NDC: | 50021-016-01 |
| Package Description: | 235 g in 1 TUBE (50021-016-01) |
NDC Information of Sunzone Family SPF 15
| NDC Code | 50021-016-01 |
| Proprietary Name | Sunzone Family SPF 15 |
| Package Description | 235 g in 1 TUBE (50021-016-01) |
| Product NDC | 50021-016 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Avobenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121114 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Empack Spraytech Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE |
| Strength Number | 1.18; 2.35 |
| Strength Unit | g/235g; g/235g |
| Pharmaceutical Classes |
