| NDC Code | 69751-101-12 |
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| Package Description | 12 APPLICATOR in 1 BOX (69751-101-12) / 5 g in 1 APPLICATOR (69751-101-01) |
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| Product NDC | 69751-101 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Phexx |
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| Non-Proprietary Name | Lactic Acid, L-, Citric Acid Monohydrate, And Potassium Bitartrate |
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| Dosage Form | GEL |
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| Usage | VAGINAL |
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| Start Marketing Date | 20200801 |
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| Marketing Category Name | NDA |
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| Application Number | NDA208352 |
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| Manufacturer | Evofem, Inc. |
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| Substance Name | CITRIC ACID MONOHYDRATE; LACTIC ACID, L-; POTASSIUM BITARTRATE |
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| Strength | 50; 90; 20 |
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| Strength Unit | mg/5g; mg/5g; mg/5g |
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| Pharmacy Classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE] |
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