| Product NDC: | 28691-1234 |
| Proprietary Name: | Alcohol swab |
| Non Proprietary Name: | Alcohol swab |
| Active Ingredient(s): | .7 mL/mL & nbsp; Alcohol swab |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SWAB |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 28691-1234 |
| Labeler Name: | Pharmaplast SAE |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20070101 |
| Package NDC: | 28691-1234-1 |
| Package Description: | 1 mL in 1 PACKET (28691-1234-1) |
| NDC Code | 28691-1234-1 |
| Proprietary Name | Alcohol swab |
| Package Description | 1 mL in 1 PACKET (28691-1234-1) |
| Product NDC | 28691-1234 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Alcohol swab |
| Dosage Form Name | SWAB |
| Route Name | TOPICAL |
| Start Marketing Date | 20070101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Pharmaplast SAE |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |