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Avant EX
Avant EX - 68306-104-02 - (Alcohol)
Drug Information of Avant EX
| Product NDC: | 68306-104 |
| Proprietary Name: | Avant EX |
| Non Proprietary Name: | Alcohol |
| Active Ingredient(s): | 70 mL/100mL & nbsp; Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Avant EX
| Product NDC: | 68306-104 |
| Labeler Name: | B4 Ventures LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100515 |
Package Information of Avant EX
| Package NDC: | 68306-104-02 |
| Package Description: | 1000 mL in 1 POUCH (68306-104-02) |
NDC Information of Avant EX
| NDC Code | 68306-104-02 |
| Proprietary Name | Avant EX |
| Package Description | 1000 mL in 1 POUCH (68306-104-02) |
| Product NDC | 68306-104 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Alcohol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100515 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | B4 Ventures LLC |
| Substance Name | ALCOHOL |
| Strength Number | 70 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
