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SunZone SPF-60
SunZone SPF-60 - 50021-234-01 - (Avobenzone and Octinoxate)
Drug Information of SunZone SPF-60
| Product NDC: | 50021-234 |
| Proprietary Name: | SunZone 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) |
Labeler Information of SunZone SPF-60
| Product NDC: | 50021-234 |
| 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 Information of SunZone SPF-60
| Package NDC: | 50021-234-01 |
| Package Description: | 234 g in 1 TUBE (50021-234-01) |
NDC Information of SunZone SPF-60
| NDC Code | 50021-234-01 |
| Proprietary Name | SunZone SPF-60 |
| Package Description | 234 g in 1 TUBE (50021-234-01) |
| Product NDC | 50021-234 |
| 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 |
