| NDC Code | 10157-2126-1 |
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| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (10157-2126-1) / 26 g in 1 TUBE, WITH APPLICATOR |
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| Product NDC | 10157-2126 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Tucks Triple Relief Hemorrhoidal |
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| Non-Proprietary Name | White Petrolatum, Glycerin, Pramoxine Hydrochloride, And Phenylephrine Hydrochloride |
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| Dosage Form | CREAM |
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| Usage | TOPICAL |
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| Start Marketing Date | 20250106 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M015 |
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| Manufacturer | Blistex Inc. |
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| Substance Name | GLYCERIN; PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE; WHITE PETROLATUM |
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| Strength | 15; .25; 1; 16 |
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| Strength Unit | g/100g; g/100g; g/100g; g/100g |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC], alpha-1 Adrenergic Agonist [EPC] |
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