| NDC Code | 17433-9883-5 |
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| Package Description | 5 TUBE in 1 BOX (17433-9883-5) > 5 mL in 1 TUBE (17433-9883-1) |
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| Product NDC | 17433-9883 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Docusol Plus |
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| Non-Proprietary Name | Docusate Sodium W/benzocaine |
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| Dosage Form | LIQUID |
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| Usage | RECTAL |
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| Start Marketing Date | 20130712 |
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| End Marketing Date | 20241031 |
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| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
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| Application Number | part334 |
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| Manufacturer | Enemeez LLC DBA Summit Pharmaceuticals |
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| Substance Name | BENZOCAINE; DOCUSATE SODIUM |
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| Strength | 20; 283 |
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| Strength Unit | mg/5mL; mg/5mL |
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| Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
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