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Mango
Mango - 57691-566-60 - (Alcohol)
Drug Information of Mango
| Product NDC: | 57691-566 |
| Proprietary Name: | Mango |
| Non Proprietary Name: | Alcohol |
| Active Ingredient(s): | .734 g/mL & nbsp; Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mango
| Product NDC: | 57691-566 |
| Labeler Name: | The Body Shop Wake Forest |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100915 |
Package Information of Mango
| Package NDC: | 57691-566-60 |
| Package Description: | 60 mL in 1 BOTTLE (57691-566-60) |
NDC Information of Mango
| NDC Code | 57691-566-60 |
| Proprietary Name | Mango |
| Package Description | 60 mL in 1 BOTTLE (57691-566-60) |
| Product NDC | 57691-566 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Alcohol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100915 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | The Body Shop Wake Forest |
| Substance Name | ALCOHOL |
| Strength Number | .734 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
