water - Medications

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Uses washes the eye to help relieve irritation discomfort burning stinging itching by removing loose foreign material air pollutants (smog or pollen) chlorinated water

Uses washes the eye to help relieve • irritation • stinging • discomfort • itching • burning by removing • loose foreign material • air pollutants (smog or pollen) • chlorinated water

​Use For cleansing the eye to help relieve irritaion or burning by removing loose foreign material

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Use A preservative for use in potable self-contained emergency eyewash stations

Use For cleansing the eye to help relieve irritation by removing loose foreign material

Uses: For temporary relief of minor: irritability* anger* fatigue* inflexibility* impatience* bitter taste* headache* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Uses: For temporary relief of minor: feelings of anguish* worry* restlessness* inability to let go of obsessions* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Uses For flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination

Uses For flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

FLOLAN (epoprostenol sodium) for injection is sterile sodium salt that is a white or off-white powder formulated for intravenous (IV) administration. Each vial of FLOLAN contains epoprostenol sodium equivalent to either 0.5 mg (500,000 ng) or 1.5 mg (1,500,000 ng) epoprostenol, 3.76 mg glycine, 50 mg mannitol, and 2.93 mg sodium chloride. Sodium hydroxide may have been added to adjust pH. Epoprostenol (PGI 2 , PGX, prostacyclin), a metabolite of arachidonic acid, is a naturally occurring prostaglandin with potent vasodilatory activity and inhibitory activity of platelet aggregation. The chemical name of epoprostenol is (5Z,9α,11α,13 E ,15 S )-6,9-epoxy-11,15-dihydroxyprosta-5,13-dien-1-oic acid. Epoprostenol sodium has a molecular weight of 374.45 and a molecular formula of C 20 H 31 NaO 5 . The structural formula is: FLOLAN must be reconstituted with pH 12 STERILE DILUENT for FLOLAN. pH 12 STERILE DILUENT for FLOLAN is supplied in plastic vials each containing 50 mL of 94 mg glycine, 73.3 mg sodium chloride, sodium hydroxide (added to adjust the pH to 11.7 to 12.3), and Water for Injection. The stability of reconstituted solutions of FLOLAN is pH-dependent and is greater at higher pH. epoprostenol sodium chemical structure

USES: • For the temporary relief of the symptoms including: • exhaustion • gastrointestinal support • fatigue • irregular bowels These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material.

For topical irrigation of eyes, burns and wounds

Insulin lispro is a rapid-acting human insulin analog produced by recombinant DNA technology utilizing a non-pathogenic laboratory strain of Escherichia coli . Insulin lispro differs from human insulin in that the amino acid proline at position B28 is replaced by lysine and the lysine in position B29 is replaced by proline. Chemically, it is Lys(B28), Pro(B29) human insulin analog and has the empirical formula C 257 H 383 N 65 O 77 S 6 and a molecular weight of 5.808 kDa, both identical to that of human insulin. Insulin lispro has the following primary structure: HUMALOG (insulin lispro) injection is a sterile, clear, and colorless solution for subcutaneous or intravenous use. Each mL of HUMALOG U-100 contains 100 units of insulin lispro, and the inactive ingredients: dibasic sodium phosphate (1.0 mg), glycerin (16 mg), metacresol (3.15 mg), trace amounts of phenol, zinc oxide (content adjusted to provide 0.0197 mg zinc ion), and Water for Injection, USP. Each mL of HUMALOG U-200 contains 200 units of insulin lispro, and the inactive ingredients: glycerin (16 mg), metacresol (3.15 mg), trace amounts of phenol, tromethamine (5 mg), zinc oxide (content adjusted to provide 0.046 mg zinc ion), and Water for Injection, USP. HUMALOG has a pH of 7.0 to 7.8. Hydrochloric acid 10% and/or sodium hydroxide 10% is added to adjust the pH. Primary Structure

Insulin aspart-xjhz is a rapid-acting human insulin analog homologous with regular human insulin with the exception of a single substitution of the amino acid proline by aspartic acid in position B28 and is produced by recombinant DNA technology utilizing Pichia pastoris . Insulin aspart-xjhz has the empirical formula C 256 H 381 N 65 O 79 S 6 and a molecular weight of 5825.8 Da. Figure 1. Structural formula of insulin aspart-xjhz. KIRSTY (insulin aspart-xjhz) injection is a sterile, clear, and colorless solution for subcutaneous or intravenous use. Each mL contains 100 units of insulin aspart-xjhz, and the inactive ingredients dibasic sodium phosphate (0.997 mg), glycerin (16 mg), m -cresol (1.72 mg), phenol (1.50 mg), sodium chloride (0.58 mg), zinc (19.6 mcg), and Water for Injection, USP. KIRSTY has a pH of 7.0-7.8. Hydrochloric acid 1% and/or sodium hydroxide 1% may be added to adjust pH. Figure 1. Structural formula of insulin aspart-xjhz

Insulin aspart is a rapid-acting human insulin analog homologous with regular human insulin with the exception of a single substitution of the amino acid proline by aspartic acid in position B28, and is produced by recombinant DNA technology utilizing Saccharomyces cerevisiae (baker's yeast). Insulin aspart has the empirical formula C 256 H 381 N 65 0 79 S 6 and a molecular weight of 5825.8 Da. Figure 1. Structural formula of insulin aspart. NOVOLOG (insulin aspart) injection is a sterile, clear, and colorless solution for subcutaneous or intravenous use. Each mL contains 100 units of insulin aspart and the inactive ingredients: disodium hydrogen phosphate dihydrate (1.25 mg), glycerin (16.0 mg), metacresol (1.72 mg), phenol (1.50 mg), sodium chloride (0.58 mg), zinc (19.6 mcg), and Water for Injection, USP. NOVOLOG has a pH of 7.2-7.6. Hydrochloric acid 10% and/or sodium hydroxide 10% may be added to adjust pH. Fig. 1 - Structural Formula of Insulin Aspart

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Uses washes the eye to help relieve irritation discomfort burning stinging itching by removing loose foreign material air pollutants (smog or pollen) chlorinated water

Questions or Comments? Call 800.570.0021 Between 9am-5pm PST [email protected] siddhaflowers.com MFD by Siddha Flower Essences Oxnard, CA 93030 Made in USA Side Panel flower essences and homeopathy: Jump start your body's natural ability to heal Natural, safe and non-habit forming No contraindications. May be effectively used with drugs and other supplements Alcohol, sugar, dairy and gluten free Prepared in purified water with natural preservatives Blends time-tested natural medicine with modern technology One month supply FOUNDATIONAL REMEDIES may be used with targeted remedies stress relief daily alignment emotional detox deep-seated stress TARGETED REMEDIES sleep male balance healthy hair blood sugar female balance lung and sinus muscles and joints throat and voice youthful skin teeth and gums happy heart hearing digest sight

Uses washes the eye to help relieve irritation discomfort burning stinging itching by removing loose foreign material air pollutants (smog or pollen) chlorinated water

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign materia.

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material.

USES: May temporarily relieve emotional conflicts.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Use: for cleaning the eye to help relieve irritation, discomfort, burning, stinging, smarting or itching by removing loose foreign material, air pollutants (smog or pollen) or chlorinated water.

USES: • For the temporary relief from symptoms including: • self induced vertigo • light sensitivity • mood swings • poor memory These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Uses For rinsing the eyes to reduce risk of severe injury caused by acid or alkali

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Apply directly to a toothbrush to clean your mouth

Uses For rinsing the eyes to reduce risk of severe injury caused by chemicals or particulate contamination

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Uses washes the eye to help relieve irritation discomfort burning stinging itching by removing loose foreign material air pollutants (smog or pollen) chlorinated water

INDICATIONS: To aid with proper hydration.

INDICATIONS: To aid with proper hydration.

Remodulin (treprostinil) Injection is a sterile solution of treprostinil, a prostacyclin mimetic, formulated for subcutaneous or intravenous administration. Remodulin is supplied in 20-mL multidose vials in eight strengths, containing 2 mg (0.1 mg/mL), 4 mg (0.2 mg/mL), 8 mg (0.4 mg/mL), 20 mg (1 mg/mL), 50 mg (2.5 mg/mL), 100 mg (5 mg/mL), 200 mg (10 mg/mL), or 400 mg (20 mg/mL) of treprostinil. Each mL also contains 5.3 mg sodium chloride (except for the 10 mg/mL and 20 mg/mL strengths, which contain 4.0 mg sodium chloride), 3 mg metacresol, 6.3 mg sodium citrate dihydrate, and water for injection. Sodium hydroxide and hydrochloric acid may be added to adjust pH between 6.0 and 7.2. Treprostinil is chemically stable at room temperature and neutral pH. Treprostinil is (1 R ,2 R ,3a S ,9a S )-[[2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-[(3 S )-3-hydroxyoctyl]-1 H -benz[ f ]inden-5-yl]oxy]acetic acid. Treprostinil has a molecular weight of 390.52 and a molecular formula of C 23 H 34 O 5 . The structural formula of treprostinil is: Sterile Diluent for Remodulin is a high-pH (pH~10.4) glycine diluent supplied in a 50-mL vial containing 50 mL of Sterile Diluent for Remodulin. Each vial contains 94 mg glycine, 73.3 mg sodium chloride, sodium hydroxide (to adjust pH), and water for injection. Chemical Structure

Uses washes the eye to help relieve irritation stinging discomfort itching burning by removing loose foreign material air pollutants(smog or pollen) chlorinated water

Uses washes the eye to help relieve irritation discomfort burning stinging itching by removing loose foreign material air pollutants (smog or pollen) chlorinated water

Uses washes the eye to help relieve irritation discomfort burning stinging itching by removing loose foreign material air pollutants (smog or pollen) chlorinated water

Treprostinil Injection is a sterile solution of treprostinil formulated for subcutaneous or intravenous administration. Treprostinil injection is supplied in 20 mL multidose vials in four strengths, containing 20 mg, 50 mg, 100 mg, or 200 mg (1 mg/mL, 2.5 mg/mL, 5 mg/mL or 10 mg/mL) of treprostinil. Each mL also contains 5.3 mg sodium chloride (except for the 10 mg/mL strength which contains 4.0 mg sodium chloride), 3 mg metacresol, 6.3 mg sodium citrate dihydrate, and water for injection. Sodium hydroxide and hydrochloric acid may be added to adjust pH between 6.0 and 7.2. Treprostinil is chemically stable at room temperature and neutral pH. Treprostinil is (1 R ,2 R ,3a S ,9a S )-[[2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-[(3 S )-3-hydroxyoctyl]-1 H -benz[ f ]inden-5-yl]oxy]acetic acid monohydrate. Treprostinil has a molecular weight of 408.53 and a molecular formula of C 23 H 34 O 5 .H 2 O. The structural formula of treprostinil is: Sterile Diluent for Tresprostinil Injection is a high-pH (pH-10.4) glycine diluent supplied in a 50 mL vial containing 50 mL of Sterile Diluent for Tresprostinil Injection. Each vial contains 94 mg glycine, 73.3 mg sodium chloride, sodium hydroxide ( to adjust pH), and water for injection. Chemical Structure

This preparation is designed solely for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection. Sterile Water for Injection, USP is a sterile, nonpyrogenic preparation of water for injection which contains no bacteriostat, antimicrobial agent or added buffer and is supplied only in single-dose containers to dilute or dissolve drugs for injection. For I.V. injection, add sufficient solute to make an approximately isotonic solution. Water for Injection, USP is chemically designated H 2 O. The glass vial is Type I or II borosilicate glass and meets the requirements of the powdered glass test according to the USP standards. The semi-rigid vial 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 labeled volume.