USP purified water

Vehicles. Ophthalmic drops are, with few exceptions, aqueous fluids using purified water USP as the solvent. Water for injection is not required as it is in parenterals. Purified water meeting USP standards may... 

Pediatric powder for oral solution Prior to dispensing, the pharmacist must constitute dry powder with Purified Water, USP, to an initial concentration of 20 mg/mL and immediately mix the resulting solution with antacid to a final concentration of 10 mg/mL as follows ... 

Bacterial Endotoxins Test (85)," "Biological Reactivity Tests, in vivo (88)," "Particulate Matter in Injections (788)," and "Purified Water," USP 23, The U.S. Pharmacopeial Convention, Rockville, Md., 1994. 

A complete list of components for the product. Typically, this list is part of the bill of materials (BOM). This list should be comprehensive, including those raw materials that may not show up in the final dosage form or on the BOM (e.g., purified water, USP). 

The importance of selecting gravimetry instead of volumetry to measure liquid amounts in the pharmaceutical industry of liquid dosage forms is well illustrated by the volume contraction of water-ethanol and volume expansion of ethyl acetate-carbon disulfide liquid mixtures as well as a CS2-ethyl acetate system. The National Formulary (NF) diluted alcohol is a typical example of the volume nonadditivity of liquid mixtures [29], This solution is prepared by mixing equal volumes of alcohol [U.S. Pharmacopeia (USP)] USP and purified water (USP). The final volume of this solution is about 3% less than the sum of the individual volumes because of the contraction due to the mixing phenomenon [1], In addition, molecular interactions of surfactants in mixed monolayers at the air-aqueous solution interface and in mixed micelles in aqueous media also cause some contraction of volume upon mixing [30],... 

Purified water USP Distillation or ion exchange No Pharmaceutical solvent... 

HC1 in a white cream base of purified water USP, propylene glycol dicaprylate, glycerin USP, cetyl alcohol NF, glyceryl monostearate SE, white petrolatum USP, stearic acid NF, polyoxyethylene cetyl ether, benzyl alcohol NF, diethanolamine NF, and sodium benzoate NF. 

Cream 0.77% and lotion 0.77% are for topical use. Each gram of cream contains 7.70 mg ciclopirox (as ciclopirox olamine) in a water-miscible vanishing-cream base consisting of purified water USP, cetyl alcohol NF, mineral oil USP, octyldodecanol NF, stearyl alcohol NF, cocamide DEA, polysorbate 60 NF, myristyl alcohol NF, sorbitan monostearate NF, lactic acid USP, and benzyl alcohol NF (1%) as preservative. Each gram of lotion contains 7.70 mg ciclopirox (as ciclopirox olamine) in a water-miscible lotion base consisting of purified water USP, cocamide DEA, octyldodecanol NF, mineral oil USP, stearyl alcohol... 

Desoximetasone emollient cream 0.25%, desoximetasone gel 0.05%, desoximetasone ointment 0.25%, and desoximetasone emollient cream 0.05% contain the active synthetic corticosteroid desoximetasone. The topical corticosteroids constitute a class of primarily synthetic steroids used as anti-inflammatory and antipruritic agents. Each gram of emollient cream 0.25% contains 2.5 mg desoximetasone in an emollient cream consisting of white petrolatum USP, purified water USP, isopropyl myristate NF, lanolin alcohols NF, mineral oil USP, cetostearyl alcohol NF, aluminum stearate, and magnesium stearate. Each gram of gel 0.05% contains 0.5 mg desoximetasone in a gel consisting of purified water USP, SD alcohol 40 (20%... 

Each gram of 4% cream contains 40 mg of hydroquinone USP in a vanishing-cream base of purified water USP, stearic acid NF, propylene glycol USP, polyoxyl 40 stearate NF, polyoxyethylene (25) propylene glycol stearate, glycerol monostearate, light mineral oil NF, squalane NF, propylparaben NF, and sodium metabisulfite NF. 

Each gram of 4% gel contains 40 mg hydroquinone USP, 50 mg padimate O USP, and 30 mg dioxybenzone USP in a hydro-alcoholic base of alcohol USP, purified water USP, propylene glycol USP, entprol, carbomer 940, edetate disodium USP, and sodium metabisulfite NF. 

The cream and lotion formulations contain the antifungal active compound oxiconazole nitrate. Both formulations are for topical dermatologic use only. The cream contains 10 mg oxiconazole per gram of cream in a white to off-white, opaque cream base of purified water USP, white petrolatum USP, stearyl alcohol NF, propylene glycol USP, polysorbate 60 NF, and cetyl alcohol NF, with benzoic... 

The ointment is an enzymatic debriding-healing ointment that contains standardized papain USP (not less than 521,700 USP units per gram of ointment), urea USP 10%, and chlorophyllin copper complex sodium 0.5% in a hydrophilic base composed of purified water USP, propylene glycol USP, white petrolatum USP, stearyl alcohol NF, polyoxyl 40 stearate NF, sorbitan monostearate NF, boric acid NF, chlorobutanol (anhydrous) NF (as a pre-... 

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