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Freshorize
Freshorize - 52305-200-20 - (Alcohol)
Drug Information of Freshorize
| Product NDC: | 52305-200 |
| Proprietary Name: | Freshorize |
| Non Proprietary Name: | Alcohol |
| Active Ingredient(s): | 185 mL/295mL & nbsp; Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Freshorize
| Product NDC: | 52305-200 |
| Labeler Name: | Freshorize, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100601 |
Package Information of Freshorize
| Package NDC: | 52305-200-20 |
| Package Description: | 295 mL in 1 BOTTLE, PUMP (52305-200-20) |
NDC Information of Freshorize
| NDC Code | 52305-200-20 |
| Proprietary Name | Freshorize |
| Package Description | 295 mL in 1 BOTTLE, PUMP (52305-200-20) |
| Product NDC | 52305-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Alcohol |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Freshorize, Ltd. |
| Substance Name | ALCOHOL |
| Strength Number | 185 |
| Strength Unit | mL/295mL |
| Pharmaceutical Classes |
