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Skintegrity Foaming Hand Sanitizer
Skintegrity Foaming Hand Sanitizer - 53329-975-84 - (Ethyl Alcohol)
Drug Information of Skintegrity Foaming Hand Sanitizer
| Product NDC: | 53329-975 |
| Proprietary Name: | Skintegrity Foaming Hand Sanitizer |
| Non Proprietary Name: | Ethyl Alcohol |
| Active Ingredient(s): | 62 mL/100mL & nbsp; Ethyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Skintegrity Foaming Hand Sanitizer
| Product NDC: | 53329-975 |
| Labeler Name: | Medline Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110408 |
Package Information of Skintegrity Foaming Hand Sanitizer
| Package NDC: | 53329-975-84 |
| Package Description: | 1000 mL in 1 BAG (53329-975-84) |
NDC Information of Skintegrity Foaming Hand Sanitizer
| NDC Code | 53329-975-84 |
| Proprietary Name | Skintegrity Foaming Hand Sanitizer |
| Package Description | 1000 mL in 1 BAG (53329-975-84) |
| Product NDC | 53329-975 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ethyl Alcohol |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110408 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Medline Industries, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | 62 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
