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ACTIPREP
ACTIPREP - 0064-1011-02 - (ETHYL ALCOHOL)
Drug Information of ACTIPREP
| Product NDC: | 0064-1011 |
| Proprietary Name: | ACTIPREP |
| Non Proprietary Name: | ETHYL ALCOHOL |
| Active Ingredient(s): | .79 mL/mL & nbsp; ETHYL ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACTIPREP
| Product NDC: | 0064-1011 |
| Labeler Name: | HEALTHPOINT, LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20011001 |
Package Information of ACTIPREP
| Package NDC: | 0064-1011-02 |
| Package Description: | 59 mL in 1 BOTTLE, PLASTIC (0064-1011-02) |
NDC Information of ACTIPREP
| NDC Code | 0064-1011-02 |
| Proprietary Name | ACTIPREP |
| Package Description | 59 mL in 1 BOTTLE, PLASTIC (0064-1011-02) |
| Product NDC | 0064-1011 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ETHYL ALCOHOL |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20011001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | HEALTHPOINT, LTD |
| Substance Name | ALCOHOL |
| Strength Number | .79 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
