| NDC Code | 10157-2127-1 |
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| Package Description | 1 TUBE in 1 CARTON (10157-2127-1) / 11.9 g in 1 TUBE |
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| Product NDC | 10157-2127 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Kanka Triple Action |
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| Non-Proprietary Name | Benzocaine And Menthol, Unspecified Form |
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| Dosage Form | GEL |
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| Usage | ORAL |
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| Start Marketing Date | 20250106 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M022 |
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| Manufacturer | Blistex Inc. |
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| Substance Name | BENZOCAINE; MENTHOL, UNSPECIFIED FORM |
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| Strength | 20; 2 |
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| Strength Unit | g/100g; g/100g |
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| Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
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