guardian drug company - Medication Listings

USE(S) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

USE(S) temporarily: relieves minor aches and pains due to the common cold, flu, sore throat, headache and toothache reduces fever

USE(S) temporarily: relieves minor aches and pains due to the common cold, flu, sore throat, headache and toothache reduces fever

USE(S) temporarily: reduces fever relieves minor aches and pains due to the common cold, flu, sore throat, headaches and toothaches

Uses relieves acid indigestion heartburn

Uses temporarily relieves cough due to minor bronchial irritation as may occur with a cold, and nasal congestion due to the common cold, hay fever or other upper respiratory allergies temporarily relieves these symptoms due to hay fever (allergic rhinitis): sneezing itching of the nose or throat runny nose itchy, watery eyes temporarily restores freer breathing through the nose

Uses temporarily relieves these common cold and flu symptoms: nasal congestion stuffy nose cough due to minor throat and minor bronchial irritation the intensity of coughing the impulse to cough to help your child get to sleep minor aches and pains sore throat headache temporarily reduces fever helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive

Uses helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive temporarily relieves: cough due to minor throat and bronchial irritation as may occur with a cold or inhaled irritants the intensity of coughing the impulse to cough to help your child get to sleep nasal congestion due to a cold stuffy nose

Diatrizoate Meglumine and Diatrizoate Sodium Solution USP is a palatable lemon-flavored water-soluble iodinated radiopaque contrast medium for oral or rectal administration only. Each mL contains 660 mg diatrizoate meglumine and 100 mg diatrizoate sodium; pH has been adjusted to 6.0 to 7.6 with sodium hydroxide. Each mL contains approximately 4.8 mg (0.21 mEq) sodium and 367 mg organically bound iodine. Inactive ingredients: edetate disodium, flavor, hydrochloric acid, polysorbate 80, purified water, saccharin sodium, simethicone, sodium citrate and sodium hydroxide. Diatrizoate meglumine is designated chemically as 1-deoxy-1-(methylamino)-D-glucitol 3,5-diacetamido-2,4,6-triiodo-benzoate (salt); diatrizoate sodium is monosodium 3, 5-diacetamido-2,4,6-triiodobenzoate. Structural formulas: Diatrizoate Meglumine C 11 H 9 I 3 N 2 O 4 .C 7 H 17 NO 5 MW 809.13 Organically Bound Iodine: 47.1% CAS – 131-49-7 Diatrizoate Sodium C 11 H 8 I 3 N 2 NaO 4 MW 635.90 Organically Bound Iodine: 59.9% CAS – 737-31-5 111 112

Uses relieves: constipation helps restore and maintain regularity promotes normal function of the bowel this product generally produces bowel movement in 12 to 72 hours

USE(S) relieves: pressure bloating symptoms referred to as gas

USE(S) relieves: acid indigestion heartburn

USE(S) helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

USE(S) relieves: acid indigestion heartburn

USE(S) relieves: acid indigestion heartburn

USE(S) relieves: acid indigestion heartburn

USE(S) relieves: diarrhea heartburn indigestion nausea upset stomach associated with these symptoms

USE(S) relieves: diarrhea heartburn indigestion nausea upset stomach associated with these symptoms

USE(S) relieves: acid indigestion heartburn

USE(S) relieves: acid indigestion heartburn

Levetiracetam oral solution, USP is an antiepileptic drug available as a clear, colorless to pale yellow, grape-flavored liquid (100 mg/mL) for oral administration. The chemical name of levetiracetam, a single enantiomer, is (-)-(S)-α-ethyl-2-oxo-1-pyrrolidineacetamide, its molecular formula is C8H14N2O2 and its molecular weight is 170.21. Levetiracetam is chemically unrelated to existing antiepileptic drugs (AEDs). It has the following structural formula: Levetiracetam, USP is a white to off-white powder with a faint odor and a bitter taste. It is very soluble in water and acetonitrile and practically insoluble in hexane. Levetiracetam oral solution, USP contains 100 mg of levetiracetam, USP per mL. Inactive ingredients: acesulfame potassium, anhydrous citric acid, artificial grape flavor, glycerin, magnasweet, maltitol, methylparaben, propylparaben, purified water, sodium citrate dihydrate. structure-1.jpg

USE(S) relieves symptoms of diarrhea plus bloating, pressure and cramps, commonly referred to as gas

USE(S) relieves: diarrhea heartburn indigestion nausea upset stomach associated with these symptoms

Uses helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive temporarily relieves: cough due to minor throat and bronchial irritation as may occur with a cold or inhaled irritants the intensity of coughing the impulse to cough to help you get to sleep

USE(S) helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

USE(S) for relief of occasional sleeplessness helps you to fall asleep if you have difficulty falling asleep

Omeprazole and Sodium Bicarbonate capsules are a combination of omeprazole, a proton-pump inhibitor, and sodium bicarbonate, an antacid. Omeprazole is a substituted benzimidazole, 5-methoxy-2- [[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, a racemic mixture of two enantiomers that inhibits gastric acid secretion. Its empirical formula is C17H19N3O3S, with a molecular weight of 345.42. The structural formula is: Omeprazole is a white to off-white crystalline powder which melts with decomposition at about 155ºC. It is a weak base, freely soluble in ethanol and methanol, and slightly soluble in acetone and isopropanol and very slightly soluble in water. The stability of omeprazole is a function of pH; it is rapidly degraded in acid media but has acceptable stability under alkaline conditions. Omeprazole and Sodium Bicarbonate capsules are supplied as immediate-release capsules. Each capsule contains either 40 mg or 20 mg of omeprazole and 1100 mg of sodium bicarbonate with the following excipients: croscarmellose sodium and sodium stearyl fumarate. The capsule shell contains gelatin, titanium dioxide and the colorants FD&C Blue # 1, FD&C Red # 3, FD&C Red 40 and the components of blue imprinting edible ink are TekPrintTM SB-6003 Blue Ink (butyl alcohol, dehydrated alcohol, FD&C Blue # 2 aluminum lake, isopropyl alcohol, propylene glycol, shellac, strong ammonium solution). Omeprazole and Sodium Bicarbonate capsules are immediate-release formulations that contain sodium bicarbonate which raises the gastric pH and thus protects omeprazole from acid degradation. 2

Uses relieves: diarrhea heartburn indigestion nausea upset stomach associated with these symptoms

Potassium Chloride is a white to almost white crystalline powder or colorless crystals. It is soluble in water and slightly soluble in alcohol. Chemically, Potassium Chloride is K-Cl with a molecular mass of 74.55. Oral Solution: 10%: Each 15 mL of solution contains 1.5 g of potassium chloride, USP and the following inactive ingredients: citric acid anhydrous, FD&C Yellow #6, glycerin, methylparaben, orange flavor, propylene glycol, propylparaben, purified water, sodium citrate dihydrate, sucralose. Oral Solution 20%: Each 15 mL of solution contains 3.0 g of potassium chloride, USP and the following inactive ingredients: citric acid anhydrous, FD&C Yellow #6, glycerin, methylparaben, orange flavor, propylene glycol, propylparaben, purified water, sodium citrate dihydrate, sucralose.

Potassium Chloride is a white crystalline or colorless solid. It is soluble in water and slightly soluble in alcohol. Chemically, Potassium Chloride is K-Cl with a molecular mass of 74.55. Each pouch of light pink to orange powder contains 1.5 g of potassium chloride, USP, which is equivalent to potassium 20 mEq and chloride 20 mEq and the following inactive ingredients: citric acid anhydrous, colloidal silicon dioxide, FD&C Yellow #6, orange flavor powder, and sucralose.

Uses relieves: occasional constipation (irregularity)

Uses temporarily relieves these common cold and flu symptoms: nasal congestion sinus congestion and pressure minor aches and pains sore throat headache temporarily reduces fever helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive

Uses temporarily relieves these common cold and flu symptoms: nasal congestion sinus congestion and pressure cough due to minor throat and minor bronchial irritation minor aches and pains sore throat headache temporarily reduces fever temporarily promotes nasal and/or sinus drainage helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive

Uses hepls loosen phelgm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive temporarily relieves: cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the intensity of coughing the impulse to cough to help you get to sleep nasal congestion due to a cold

USE(S) relieves: acid indigestion heartburn

USE(S) relieves: diarrhea heartburn indigestion nausea upset stomach associated with these symptoms