SPL Set ID: 673d6a97-463d-6645-e053-2a91aa0a1435

1 drug(s) with this SPL Set ID

Open DailyMed details

NuDroxiPAK DSDR-50 Diclofenac Sodium, Methyl Salicylate/Menthol/Capsaicin NuDroxicin pain relief Roll-On Methyl Salicylate, Menthol, Capsaicin MAGNESIUM SULFATE, UNSPECIFIED FORM CAPSAICIN CAPSAICIN WATER ARNICA MONTANA FLOWER ETHYLHEXYLGLYCERIN INDIAN FRANKINCENSE CARBOXYPOLYMETHYLENE CETEARYL OLIVATE DIMETHYL SULFONE MENTHOL MENTHOL POLYSORBATE 20 YELLOW WAX GLYCERYL MONOSTEARATE ILEX PARAGUARIENSIS LEAF SORBITAN OLIVATE PHENOXYETHANOL METHYL SALICYLATE SALICYLIC ACID Diclofenac Sodium Diclofenac Sodium POLYETHYLENE GLYCOL, UNSPECIFIED PROPYLENE GLYCOL SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO STEARIC ACID FERROSOFERRIC OXIDE TITANIUM DIOXIDE DICLOFENAC SODIUM DICLOFENAC HYPROMELLOSE, UNSPECIFIED LACTOSE MONOHYDRATE ANHYDROUS LACTOSE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYSORBATE 80 SODIUM ALGINATE TALC POLYVINYL ACETATE PHTHALATE ALUMINUM HYDROXIDE R;550
50 mg
OTC Limited

Diclofenac sodium delayed-release tablets, USP are a benzene-acetic acid derivative. Diclofenac sodium, USP is a white to almost white crystalline powder and is sparingly soluble in water at 25°C. The chemical name is 2-[(2,6-dichlorophenyl)amino] benzeneacetic acid, monosodium salt. The molecular weight is 318.13. Its molecular formula is C 14 H 10 Cl 2 NNaO 2 , and it has the following structural formula Each enteric-coated tablet for oral administration contains 50 mg or 75 mg of diclofenac sodium, USP. In addition, each tablet contains the following inactive ingredients: aluminum hydrate, colloidal silicon dioxide, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, polyvinyl acetate phthalate, propylene glycol, silica, sodium alginate, sodium starch glycolate (Type A), stearic acid, synthetic black iron oxide, talc, and titanium dioxide. 1

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