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CTCA Foaming Hand Sanitizer
CTCA Foaming Hand Sanitizer - 11084-701-01 - (Ethyl Alcohol)
Drug Information of CTCA Foaming Hand Sanitizer
| Product NDC: | 11084-701 |
| Proprietary Name: | CTCA Foaming Hand Sanitizer |
| Non Proprietary Name: | Ethyl Alcohol |
| Active Ingredient(s): | 70 mL/100mL & nbsp; Ethyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CTCA Foaming Hand Sanitizer
| Product NDC: | 11084-701 |
| Labeler Name: | Deb USA, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120515 |
Package Information of CTCA Foaming Hand Sanitizer
| Package NDC: | 11084-701-01 |
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (11084-701-01) |
NDC Information of CTCA Foaming Hand Sanitizer
| NDC Code | 11084-701-01 |
| Proprietary Name | CTCA Foaming Hand Sanitizer |
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (11084-701-01) |
| Product NDC | 11084-701 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ethyl Alcohol |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120515 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Deb USA, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | 70 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
