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Actigel
Actigel - 63146-301-02 - (Alcohol)
Drug Information of Actigel
| Product NDC: | 63146-301 |
| Proprietary Name: | Actigel |
| Non Proprietary Name: | Alcohol |
| Active Ingredient(s): | 534 mg/mL & nbsp; Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Actigel
| Product NDC: | 63146-301 |
| Labeler Name: | Kay Chemical Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100526 |
Package Information of Actigel
| Package NDC: | 63146-301-02 |
| Package Description: | 800 mL in 1 BAG (63146-301-02) |
NDC Information of Actigel
| NDC Code | 63146-301-02 |
| Proprietary Name | Actigel |
| Package Description | 800 mL in 1 BAG (63146-301-02) |
| Product NDC | 63146-301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Alcohol |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100526 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kay Chemical Company |
| Substance Name | ALCOHOL |
| Strength Number | 534 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
