Drugs Similar to ALCOHOL

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

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

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Indications and Usage: For use as an antiseptic

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

Uses For personal hand hygiene to help prevent the spread of bacteria, and can be used in place of hand washing if soap and water are not available.

Uses For personal hand hygine to help prevent the spread of bacteria, and can be used in place of hand washing if soap and water are not available.

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Uses For preparation of skin prior to an injection

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

Indications and Usage: Stop use and ask a doctor if: Irritation or redness develops condition persists for more than 72 hours Cleansing of an injection site

Uses: First aid to help prevent infection in minor cuts, scrapes, and burns

Uses First aid to help prevent infection in minor cuts, scrapes and burns For preparation of the skin prior to an injection

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Uses: First aid to help prevent infection in minor cuts, scrapes, and 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 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

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

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

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 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

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 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 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 ■ 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.

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

Use To help reduce bacteria on the skin.

1 DESCRIPTION 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. Chemical Structure DESCRIPTION Bupivacaine hydrochloride is 2-Piperidinecarboxamide, 1-butyl- N -(2,6-dimethylphenyl)-, monohydrochloride, monohydrate, a white crystalline powder that is freely soluble in 95 percent ethanol, soluble in water, and slightly soluble in chloroform or acetone. It has the following structural formula: Epinephrine is (-)-3,4-Dihydroxy-α-[(methylamino)methyl] benzyl alcohol. It has the following structural formula: MARCAINE is available in sterile isotonic solutions with and without epinephrine (as bitartrate) 1:200,000 for injection via local infiltration, peripheral nerve block, and caudal and lumbar epidural blocks. Solutions of MARCAINE may be autoclaved if they do not contain epinephrine. Solutions are clear and colorless. Bupivacaine is related chemically and pharmacologically to the aminoacyl local anesthetics. It is a homologue of mepivacaine and is chemically related to lidocaine. All three of these anesthetics contain an amide linkage between the aromatic nucleus and the amino, or piperidine group. They differ in this respect from the procaine-type local anesthetics, which have an ester linkage. MARCAINE —Sterile isotonic solutions containing sodium chloride. In multiple-dose vials, each mL also contains 1 mg methylparaben as antiseptic preservative. The pH of these solutions is adjusted to between 4 and 6.5 with sodium hydroxide or hydrochloric acid. MARCAINE with epinephrine 1:200,000 (as bitartrate)—Sterile isotonic solutions containing sodium chloride. Each mL contains bupivacaine hydrochloride and 0.0091 mg epinephrine bitartrate, with 0.5 mg sodium metabisulfite, 0.001 mL monothioglycerol, and 2 mg ascorbic acid as antioxidants, 0.0017 mL 60% sodium lactate buffer, and 0.1 mg edetate calcium disodium as stabilizer. In multiple-dose vials, each mL also contains 1 mg methylparaben as antiseptic preservative. The pH of these solutions is adjusted to between 3.4 and 4.5 with sodium hydroxide or hydrochloric acid. The specific gravity of MARCAINE 0.5% with epinephrine 1:200,000 (as bitartrate) at 25°C is 1.008 and at 37°C is 1.008. structural formula bupivacaine hydrochloride structural formula epinephrine

Naloxone hydrochloride, an opioid antagonist, is a synthetic congener of oxymorphone. In structure it differs from oxymorphone in that the methyl group on the nitrogen atom is replaced by an allyl group. NALOXONE HYDROCHLORIDE (-)-17-Allyl-4,5α-epoxy-3,14-dihydroxymorphinan-6-one hydrochloride Naloxone hydrochloride occurs as a white to slightly off-white powder, and is soluble in water, in dilute acids, and in strong alkali; slightly soluble in alcohol; practically insoluble in ether and in chloroform. Naloxone Hydrochloride Injection is available as a sterile solution for intravenous, intramuscular and subcutaneous administration in 1 mg/mL concentration. pH is adjusted to 3.5 ± 0.5 with hydrochloric acid. Each mL also contains 8.35 mg of sodium chloride. Naloxone Hydrochloride Injection is preservative-free. IMAGE

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

USE For preparation of the skin prior to an injection

Uses Antiseptic Cleanser Kills harmful bacteria and germs First Aid to Help Prevent Infection

Uses to decrease bacteria on fabric, clothes, hands, skin & surfaces that could cause disease for repeated use

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

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

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

Uses • to decrease bacteria on fabrics, clothes, hands, skin & surfaces that could cause disease • for repeated use

Dexamethasone sodium phosphate is a water-soluble inorganic ester of dexamethasone. It occurs as a white or slightly yellow crystalline powder, is odorless or has a slight odor of alcohol, is exceedingly hygroscopic and is freely soluble in water. Dexamethasone sodium phosphate is an adrenocortical steroid anti-inflammatory drug. Chemically, dexamethasone sodium phosphate is 9-Fluoro-11ß,17,21-trihydroxy-16α-methylpregna-1, 4-diene-3,20-dione 21-(dihydrogen phosphate) disodium salt and has the following structural formula: Dexamethasone Sodium Phosphate Injection, USP is a sterile solution of dexamethasone sodium phosphate in water for injection for intravenous (IV), intramuscular (IM), intra-articular, soft-tissue or intralesional use. Each mL contains dexamethasone sodium phosphate equivalent to dexamethasone phosphate 4 mg or dexamethasone 3.33 mg; benzyl alcohol 10 mg added as preservative; sodium citrate dihydrate 11 mg; sodium sulfite 1 mg as an antioxidant; Water for Injection q.s. Citric acid and/or sodium hydroxide may have been added for pH adjustment (7.0 to 8.5). Air in the container is displaced by nitrogen. Structure-D DESCRIPTION Bupivacaine hydrochloride is 2-Piperidinecarboxamide, 1-butyl-N-(2,6-dimethylphenyl)-, monohydrochloride, monohydrate, a white crystalline powder that is freely soluble in 95 percent ethanol, soluble in water, and slightly soluble in chloroform or acetone. It has the following structural formula: MARCAINE is available in sterile isotonic solutions with and without epinephrine (as bitartrate) 1:200,000 for injection via local infiltration, peripheral nerve block, and caudal and lumbar epidural blocks. Solutions of MARCAINE may be autoclaved if they do not contain epinephrine. Solutions are clear and colorless. Bupivacaine is related chemically and pharmacologically to the aminoacyl local anesthetics. It is a homologue of mepivacaine and is chemically related to lidocaine. All three of these anesthetics contain an amide linkage between the aromatic nucleus and the amino, or piperidine group. They differ in this respect from the procaine-type local anesthetics, which have an ester linkage. MARCAINE—Sterile isotonic solutions containing sodium chloride. In multiple-dose vials, each mL also contains 1 mg methylparaben as antiseptic preservative. The pH of these solutions is adjusted to between 4 and 6.5 with sodium hydroxide or hydrochloric acid. Structure-M

USE For preparation of the skin prior to injection

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 For preparation of the skin prior to injection

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