Drugs Similar to MEMBERS MARK

Uses For handwashing to decrease bacteria on the skin

Uses for handwashing to decrease bacteria on the skin

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

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 helps 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 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 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

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

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

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

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

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

Uses For preparation of the skin prior to an injection

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

Use (s) Hand sanitizer to help reduce bacteria that potentiallycan cause disease. For use when water and soap 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

Uses Hand sanitizer 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

USE For preparation of the skin prior to an injection

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

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

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

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

USES for preparation of the skin prior to injection

Use To help reduce bacteria on the skin.

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