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Caribbean Escape Anti Bacterial Foaming Hand
Caribbean Escape Anti Bacterial Foaming Hand - 59021-002-01 - (TRICLOSAN)
Drug Information of Caribbean Escape Anti Bacterial Foaming Hand
| Product NDC: | 59021-002 |
| Proprietary Name: | Caribbean Escape Anti Bacterial Foaming Hand |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | .3 g/100mL & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Caribbean Escape Anti Bacterial Foaming Hand
| Product NDC: | 59021-002 |
| Labeler Name: | Five Below |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130413 |
Package Information of Caribbean Escape Anti Bacterial Foaming Hand
| Package NDC: | 59021-002-01 |
| Package Description: | 225 mL in 1 BOTTLE (59021-002-01) |
NDC Information of Caribbean Escape Anti Bacterial Foaming Hand
| NDC Code | 59021-002-01 |
| Proprietary Name | Caribbean Escape Anti Bacterial Foaming Hand |
| Package Description | 225 mL in 1 BOTTLE (59021-002-01) |
| Product NDC | 59021-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130413 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Five Below |
| Substance Name | TRICLOSAN |
| Strength Number | .3 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
