Drugs Similar to QUALITY CHOICE

Use temporary relieves: ■ cough due to cold ■ occasional minor irritation or sore throat

Directions for itching of skin irritation, inflammation, and rashes: adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily children under 2 years of age: ask a doctor for external anal and genital itching, adults: when practical, clean the affected area with mild soap and warm water and rinse thoroughly gently dry by patting or blotting with toilet tissue or a soft cloth before applying apply to affected area not more than 3 to 4 times daily children under 12 years of age: ask a doctor

Use temporary relieves: ■ cough due to cold ■ occasional minor irritation or sore throat

Use temporary relieves: ■ cough due to cold ■ occasional minor irritation or sore throat

Use temporary relieves: ■ cough due to cold ■ occasional minor irritation or sore throat

Uses temporarily relieves nasal congestion due to: a cold hay fever upper respiratory allergies promotes nasal and sinus drainage temporarily relieves sinus congestion and pressure helps clear nasal passages; shrinks swollen nasal membranes

Uses for the temporarily relief nasal congestion due to: common cold hay fever upper respiratory allergies

Uses relieves: heartburn sour stomach acid indigestion upset stomach associated with these symptoms

Uses for the temporarily relief nasal congestion due to: common cold hay fever upper respiratory allergies

Directions shake well before using instill 1 or 2 drops in the affected eye(s) as needed children under 6 years of age: ask a dcotor

Directions Adults and children 2 years of age and older Remove cap and cut tip of tube. Apply a small amount of product to the cavity and around gum surrounding the teeth. Use up to 4 times daily or as directed by a dentist or doctor. Children under 12 years of age Should be supervised in the use of this product Children under 2 years of age Do not use

Use temporary relieves: ■ cough due to cold ■ occasional minor irritation or sore throat

USES relieves occasional constipation to help restore and maintain regularity this product generally produces bowel movement in 12 to 72 hours

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in minor cuts, scrapes, burns

Uses first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Use first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scarapes burns

Use first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: •minor cuts •scrapes •burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses First aid to help prevent the risk of infection in: minor cuts scrapes burns

Use first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses First aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses helps prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Use first aid to help prevent the risk of infection in: minor cuts scrapes burns

Use first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses patient preoperative skin preparation: for preparation of the skin prior to surgery helps reduce bacteria that potentially can cause skin infection

Uses patient preoperative skin preparation: for preparation of the skin prior to surgery helps reduce bacteria that potentially can cause skin infection Uses patient preoperative skin preparation: for preparation of the skin prior to surgery helps reduce bacteria that potentially can cause skin infection Uses patient preoperative skin preparation: for preparation of the skin prior to surgery helps reduce bacteria that potentially can cause skin infection

Uses first aid to help prevent the risk of infection in minor cuts, scrapes, burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Use first aid to help prevent the risk of infection in: minor cuts scrapes burns

Use first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scarapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Use first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: •minor cuts •scrapes •burns

Use first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses First aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns

Uses For preparation of the skin prior to an injection

Use (s) Hand sanitizer to help reduce bacteria that potentiallycan cause disease. For use when water and soap are not available.

USE For preparation of the skin prior to an injection

USES for preparation of the skin prior to injection

USE For preparation of the skin prior to an injection First aid to decrease germs in minor cuts, scrapes and burns

Use To help reduce bacteria on the skin.

Uses ■ Used to help reduce germ and bacteria that potentially can cause disease.

Uses Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Uses • hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available

Lidocaine Hydrochloride Injection, USP is a sterile, nonpyrogenic solution of lidocaine hydrochloride in water for injection for parenteral administration in various concentrations with characteristics as follows: Concentration 0.5% 1% 1.5% 2% mg/mL lidocaine HCl (anhyd.) 5 10 15 20 mg/mL sodium chloride 8 7 6.5 6 Multiple-dose vials contain 0.1% of methylparaben added as preservative. May contain sodium hydroxide and/or hydrochloric acid for pH adjustment. The pH is 6.5 (5.0 to 7.0). See HOW SUPPLIED section for various sizes and strengths. Lidocaine is a local anesthetic of the amide type. Lidocaine Hydrochloride, USP is chemically designated 2-(diethylamino)-N-(2,6-dimethylphenyl)-acetamide monohydrochloride monohydrate, a white powder freely soluble in water. The molecular weight is 288.82. It has the following structural formula: The semi-rigid vial used for the plastic vials is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration. image description 1.1 DESCRIPTION Triamcinolone acetonide injectable suspension, USP is a synthetic glucocorticoid corticosteroid with anti-inflammatory action. THIS FORMULATION IS SUITABLE FOR INTRAMUSCULAR AND INTRA-ARTICULAR USE ONLY. THIS FORMULATION IS NOT FOR INTRADERMAL INJECTION. Each mL of the sterile aqueous suspension provides 40 mg triamcinolone acetonide, USP, with 0.65% sodium chloride for isotonicity, 0.99% (w/v) benzyl alcohol as a preservative, 0.75% carboxymethylcellulose sodium, and 0.04% polysorbate 80 in an aqueous suspension. Sodium hydroxide or hydrochloric acid may be present to adjust pH to 5.0 to 7.5. At the time of manufacture, the air in the container is replaced by nitrogen. Triamcinolone acetonide injectable suspension, USP is supplied in vials providing 40 mg triamcinolone acetonide per mL, as 40 mg per 1 mL single-dose vial, 200 mg per 5 mL multiple-dose vial and 400 mg per 10 mL multiple-dose vial. The chemical name for triamcinolone acetonide is 9-Fluoro-11β,16,17,21-tetrahydroxypregna-1,4-diene-3,20-dione cyclic 16,17-acetal with acetone. Its structural formula is: Triamcinolone acetonide, USP occurs as a white to cream-colored, crystalline powder having not more than a slight odor and is practically insoluble in water and very soluble in alcohol. image description

Use Antiseptic wipe to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Ketorolac Tromethamine Injection, USP is a member of the pyrrolo-pyrrole group of nonsteroidal anti-inflammatory drugs (NSAIDs). The chemical name for ketorolac tromethamine is (±)-5-benzoyl-2,3-dihydro-1 H -pyrrolizine-1-carboxylic acid, compound with 2-amino-2-(hydroxymethyl)-1,3-propanediol (1:1), and the structural formula is presented in Figure 1 . FIGURE 1 C 15 H 13 NO 3 • C 4 H 11 NO 3 Ketorolac tromethamine is a racemic mixture of [-]S and [+]R ketorolac tromethamine. Ketorolac tromethamine may exist in three crystal forms. All forms are equally soluble in water. Ketorolac tromethamine has a pKa of 3.5 and an n-octanol/water partition coefficient of 0.26. The molecular weight of ketorolac tromethamine is 376.40. Ketorolac Tromethamine Injection, USP is available for intravenous (IV) or intramuscular (IM) administration as: 15 mg in 1 mL (1.5%) and 30 mg in 1 mL (3%) in sterile solution; 60 mg in 2 mL (3%) of ketorolac tromethamine in sterile solution is available for IM administration only. The solutions contain 10% (w/v) alcohol, USP, and 6.68 mg, 4.35 mg and 8.70 mg respectively, of sodium chloride in sterile water. The pH range is 6.9 to 7.9 and is adjusted with sodium hydroxide and/or hydrochloric acid. The sterile solutions are clear to slightly yellow in color. image description

Uses Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Uses For hand sanitizing to decrease bacteria on the skin.

Use (s) Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when water and soap are not available.

Directions Directions Tear open individual swab and apply product to the injection site prior to an injection.Rub skin briskly in circular motion from injection site outward

USE For preparation of the skin prior to injection

DIPRIVANR (Propofol) Injectable Emulsion, USP is a sterile, nonpyrogenic emulsion containing 10 mg/mL of propofol suitable for intravenous administration. Propofol is chemically described as 2,6-diisopropylphenol. The structural formula is: DIPRIVAN C12H18O M.W. 178.27 Propofol is slightly soluble in water and, thus, is formulated in a white, oil-in-water emulsion. The pKa is 11. The octanol/water partition coefficient for propofol is 6761:1 at a pH of 6 to 8.5. In addition to the active component, propofol, the formulation also contains soybean oil (100 mg/mL), glycerol (22.5 mg/mL), egg lecithin (12 mg/mL); and disodium edetate (0.005%); with sodium hydroxide to adjust pH. DIPRIVAN Injectable Emulsion, USP is isotonic and has a pH of 7 to 8.5. DIPRIVAN

Epinephrine Injection, USP 1 mg/mL is a sterile, nonpyrogenic solution. Each mL contains epinephrine 1 mg; sodium chloride 9 mg; sodium metabisulfite 0.9 mg added. May contain hydrochloric acid for pH adjustment. The solution contains no bacteriostat or antimicrobial agent. It is administered by the following routes: intravenous, intracardiac (left ventricular chamber), via endotracheal tube into the bronchial tree, subcutaneous or intramuscular. Epinephrine, USP is a sympathomimetic (adrenergic) agent designated chemically as 4-[1-hydroxy-2 (methylamino) ethyl]-1,2 benzenediol, a white, microcrystalline powder. It has the following structural formula: Sodium Chloride, USP is chemically designated NaCl, a white, crystalline compound freely soluble in water. Structural Formula of Epinephrine

Lidocaine Hydrochloride Injection, USP is a sterile, nonpyrogenic solution of lidocaine hydrochloride in water for injection for parenteral administration in various concentrations with characteristics as follows: Concentration 0.5% 1% 1.5% 2% mg/mL lidocaine HCl (anhyd.) 5 10 15 20 mg/mL sodium chloride 8 7 6.5 6 Multiple-dose vials contain 0.1% of methylparaben added as preservative. May contain sodium hydroxide and/or hydrochloric acid for pH adjustment. The pH is 6.5 (5.0 to 7.0). See HOW SUPPLIED section for various sizes and strengths. Lidocaine is a local anesthetic of the amide type. Lidocaine Hydrochloride, USP is chemically designated 2-(diethylamino)-N-(2,6-dimethylphenyl)-acetamide monohydrochloride monohydrate, a white powder freely soluble in water. The molecular weight is 288.82. It has the following structural formula: The semi-rigid vial used for the plastic vials is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration. image description DESCRIPTION Ketorolac Tromethamine Injection, USP is a member of the pyrrolo-pyrrole group of nonsteroidal anti-inflammatory drugs (NSAIDs). The chemical name for ketorolac tromethamine is (±)-5-benzoyl-2,3-dihydro-1 H -pyrrolizine-1-carboxylic acid, compound with 2-amino-2-(hydroxymethyl)-1,3-propanediol (1:1), and the structural formula is presented in Figure 1 . FIGURE 1 C 15 H 13 NO 3 • C 4 H 11 NO 3 Ketorolac tromethamine is a racemic mixture of [-]S and [+]R ketorolac tromethamine. Ketorolac tromethamine may exist in three crystal forms. All forms are equally soluble in water. Ketorolac tromethamine has a pKa of 3.5 and an n-octanol/water partition coefficient of 0.26. The molecular weight of ketorolac tromethamine is 376.40. Ketorolac Tromethamine Injection, USP is available for intravenous (IV) or intramuscular (IM) administration as: 15 mg in 1 mL (1.5%) and 30 mg in 1 mL (3%) in sterile solution; 60 mg in 2 mL (3%) of ketorolac tromethamine in sterile solution is available for IM administration only. The solutions contain 10% (w/v) alcohol, USP, and 6.68 mg, 4.35 mg and 8.70 mg respectively, of sodium chloride in sterile water. The pH range is 6.9 to 7.9 and is adjusted with sodium hydroxide and/or hydrochloric acid. The sterile solutions are clear to slightly yellow in color. Figure 1