sodium chloride - Medications

Uses See the leaflet enclosed for detail.

Uses See the leaflet enclosed for detail.

INDICATIONS: Our adrenal glands can become exhausted from chronic stress, worry, overwork or poor nutrition. Temporarily relieves signs of adrenal exhaustion, including: ° dizziness fatigue & weakness ° mental stress ° loss of our sense of well being ° natural ° gluten & lactose free ° no artificial flavors or colors ° no known negative side effects ° no known negative drug interactions

USES: • For the temporary relief of symptoms including: • minor breathing issues • lung support These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

BSS™ Sterile Irrigating Solution is a sterile balanced salt solution, each mL containing sodium chloride (NaCl) 0.64%, potassium chloride (KCl) 0.075%, calcium chloride dihydrate (CaCl 2 •2H 2 O) 0.048%, magnesium chloride hexahydrate (MgCl 2 •6H 2 O) 0.03%, sodium acetate trihydrate (C 2 H 3 NaO 2 •3H 2 O) 0.39%, sodium citrate dihydrate (C 6 H 5 Na 3 O 7 •2H 2 O) 0.17%, sodium hydroxide and/or hydrochloric acid (to adjust pH), and water for injection. The pH is approximately 7.5. The osmolality is approximately 300 mOsm/Kg.

BSS ™ Sterile Irrigating Solution is a sterile balanced salt solution, each mL containing sodium chloride (NaCl) 0.64%, potassium chloride (KCl) 0.075%, calcium chloride dihydrate (CaCl 2 •2H 2 O) 0.048%, magnesium chloride hexahydrate (MgCl 2 •6H 2 O) 0.03%, sodium acetate trihydrate (C 2 H 3 NaO 2 •3H 2 O) 0.39%, sodium citrate dihydrate (C 6 H 5 Na 3 O 7 •2H 2 O) 0.17%, sodium hydroxide and/or hydrochloric acid (to adjust pH), and water for injection. The pH is approximately 7.5. The osmolality is approximately 300 mOsm/Kg.

Use Temporarily relieves symptons associated with sinusitis, cold, flu, allergies Including: Post nasal drip, sneezing, runny nose, nasal stuffiness Removes inhaled irritants, dust, pollen Helps reduce swelling of nasal membranes Moistens dry nasal passages Promotes nasal and sinus clearage

USES For the temporary relief of: • Simple nervous tension • Restlessness • Trouble sleeping

INDICATIONS: For temporary relief of mild dizziness, feeling faint, aching of legs, weakness of the lower limbs, swelling of legs.

Baxter Cardioplegic Solution is a sterile, nonpyrogenic, essentially isotonic, formulation of electrolytes in Water for Injection, USP. It is a “core solution” intended for use only after addition of sodium bicarbonate to adjust pH prior to administration. After buffering with sodium bicarbonate it is suitable for cardiac instillation (usually with hypothermia) to induce arrest during open heart surgery. Other agents may be added to the solution prior to instillation (See INSTRUCTIONS FOR USE ). Each 100 mL of solution contains Calcium Chloride Dihydrate USP 17.6 mg, Magnesium Chloride, Hexahydrate USP 325.3 mg, Potassium Chloride USP 119.3 mg and Sodium Chloride USP 643 mg in Water for Injection, USP. May contain HCl and/or NaOH for pH adjustment. Electrolyte content per liter (not including ions for pH adjustment): Calcium (Ca ++ ) 2.4 mEq; Magnesium (Mg ++ ) 32 mEq; Potassium (K + ) 16 mEq; Sodium (Na + ) 110 mEq; Chloride (Cl - ) 160 mEq. Osmolar concentration, 304 mOsmol/liter (calc.); pH 3.8 (3.5 to 3.9) prior to sodium bicarbonate addition. It is required that 10 mL (840 mg) of 8.4% Sodium Bicarbonate Injection, USP (10 mEq each of sodium and bicarbonate) be added aseptically and thoroughly mixed with each 1000 mL of cardioplegic solution to adjust pH. Use 10 mL of Hospira 1 List 4900, 8.4% Sodium Bicarbonate Injection, USP, to achieve the approximate pH of 7.8 when measured at room temperature. Use of any other Sodium Bicarbonate Injection may not achieve this pH due to the varying pH’s of Sodium Bicarbonate Injections. Due to its inherent instability with other components, sodium bicarbonate must be added just prior to administration. After this addition, the solution must be stored under refrigeration and be used within 24 hours. The buffered admixture contains the following electrolytes (per liter): Ca ++ 2.4 mEq, Mg ++ 32 mEq, K + 16 mEq, Na + 120 mEq, Cl - 160 mEq and bicarbonate (HCO 3 - ) 10 mEq; osmolar concentration, 324 mOsmol/liter (calc.); pH 7.8 (approx.). If other agents are added, these values may be altered. The solution contains no bacteriostat, or antimicrobial agent and is intended only for use (after adjusting pH with sodium bicarbonate) in a single operative procedure. When smaller amounts are required, the unused portion should be discarded. Cardioplegic Solution with added sodium bicarbonate used as a coronary artery infusate induces cardiac arrest, combats ischemic ionic disturbances, buffers ischemic acidosis and protects energy sources for functional recovery after ischemia. Calcium Chloride, USP is chemically designated calcium chloride, dihydrate (CaCl 2 • 2 H 2 O), white fragments or granules freely soluble in water. Magnesium Chloride, USP is chemically designated magnesium chloride, hexahydrate (MgCl 2 • 6 H 2 O), deliquescent flakes or crystals very soluble in water. Potassium Chloride, USP is chemically designated KCl, a white granular powder freely soluble in water. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H 2 O. The flexible plastic container is fabricated from a specially formulated polyvinyl chloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C/77°F during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.

Cardioplegic Solution is a sterile, nonpyrogenic, essentially isotonic, formulation of electrolytes in water for injection. It is a "core solution" intended for use only after addition of sodium bicarbonate to adjust pH prior to administration. After buffering with sodium bicarbonate it is suitable for cardiac instillation (usually with hypothermia) to induce arrest during open heart surgery. Other agents may be added to the solution prior to instillation (See INSTRUCTIONS FOR USE ). Each 100 mL of solution contains calcium chloride, dihydrate 17.6 mg, magnesium chloride, hexahydrate 325.3 mg, potassium chloride 119.3 mg and sodium chloride 643 mg in water for injection. May contain HCl or NaOH for pH adjustment. Electrolyte content per liter (not including ions for pH adjustment): Calcium (Ca ++ ) 2.4 mEq; magnesium (Mg ++ ) 32 mEq; potassium (K + ) 16 mEq; sodium (Na + ) 110 mEq; chloride (Cl‾) 160 mEq. Osmolar concentration, 304 mOsmol/liter (calc.); pH 3.8 (3.5 to 3.9) prior to sodium bicarbonate addition. It is required that 10 mL (840 mg) of 8.4% Sodium Bicarbonate Injection, USP (10 mEq each of sodium and bicarbonate) be added aseptically and thoroughly mixed with each 1000 mL of cardioplegic solution to adjust pH. Use 10 mL of 8.4% Sodium Bicarbonate Injection, USP, to achieve the approximate pH of 7.8 when measured at room temperature. Use of any other Sodium Bicarbonate Injection may not achieve this pH due to the varying pH's of Sodium Bicarbonate Injections. Due to its inherent instability with other components, sodium bicarbonate must be added just prior to administration. After this addition, the solution must be stored under refrigeration and be used within 24 hours. The buffered admixture contains the following electrolytes (per liter): Ca ++ 2.4 mEq, Mg ++ 32 mEq, K + 16 mEq, Na + 120 mEq, Cl‾ 160 mEq and bicarbonate (HCO 3 ‾) 10 mEq; osmolar concentration, 324 mOsmol/liter (calc.); pH 7.8 (approx.). If other agents are added, these values may be altered. The solution contains no bacteriostat, or antimicrobial agent and is intended only for use (after adjusting pH with sodium bicarbonate) in a single operative procedure. When smaller amounts are required, the unused portion should be discarded. Cardioplegic Solution with added sodium bicarbonate used as a coronary artery infusate induces cardiac arrest, combats ischemic ionic disturbances, buffers ischemic acidosis and protects energy sources for functional recovery after ischemia. Calcium Chloride, USP is chemically designated calcium chloride, dihydrate (CaCl 2 • 2 H 2 O), white fragments or granules freely soluble in water. Magnesium Chloride, USP is chemically designated magnesium chloride, hexahydrate (MgCl 2 • 6 H 2 O), deliquescent flakes or crystals very soluble in water. Potassium Chloride, USP is chemically designated KCl, a white granular powder freely soluble in water. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H 2 O. The flexible plastic container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers ( free flex ® bag). Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C/77°F during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.

INDICATIONS & USAGE SECTION Formulated for symptoms such as blurred vision, light sensitivity and opacities.

INDICATIONS For the temporary relief of occasional clouded, blurred, or dim vision.*

USES: Supports healthy mineral and electrolyte balance. Improves absorption of vitamins from food. Helps replenish body with vital nutrients after strenuous workout. May decrease general pain and nervousness.* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INDICATIONS Use according to standard homeopathic indications for self-limiting conditions. Common Materia Medica indications: colds, headaches, exhaustion, minor aches and pains.*

INDICATIONS & USAGE SECTION A formulation of the 12 tissue salts for symptoms such as indigestion, exhaustion, inflammation and sensitive skin.

INDICATIONS & USAGE SECTION A formulation of the 12 tissue salts for symptoms such as indigestion, exhaustion, inflammation and sensitive skin.

INDICATIONS & USAGE SECTION A formulation of the 12 tissue salts for symptoms such as indigestion, exhaustion, inflammation and sensitive skin.

Uses Encourages healthy mineral levels and tissue repair during periods of stress, fatigue or recovery.

USES: Temporarily relieves fatigue.**

Uses Temporarily relieves the symptoms of the common cold including nasal or chest congestion, runny nose, sore throat, sneezing or cough.

Uses Temporarily relieves the symptoms of the common cold, including: nasal or chest congestion,runny nose,sore throat,sneezing cough

Uses Temporarily relieves the symptoms of the common cold including cough, runny nose, sneezing, nasal or chest congestion or sore throat with accompanying occasional sleeplessness.

INDICATIONS: May temporarily relieve symptoms due to fluid retention and anxiety.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

CLINIMIX E sulfite-free (amino acids with electrolytes in dextrose with calcium) injection for intravenous use consists of sterile, nonpyrogenic, hypertonic solutions in a dual chamber container. The outlet port chamber contains essential and nonessential amino acids with electrolytes. The formulas for the individual electrolytes and amino acids are provided in Table 8 . Table 8: Formulas for Electrolytes and Amino Acids Electrolytes Sodium Acetate C 2 H 3 NaO 2 •3H 2 O Potassium Phosphate, dibasic K 2 HPO 4 Magnesium Chloride MgCl 2 •6H 2 O Sodium Chloride NaCl Essential Amino Acids Leucine (CH 3 ) 2 CHCH 2 CH (NH 2 ) COOH Isoleucine CH 3 CH 2 CH (CH 3 ) CH (NH 2 ) COOH Valine (CH 3 ) 2 CHCH (NH 2 ) COOH Lysine (added as the hydrochloride salt) H 2 N (CH 2 ) 4 CH (NH 2 ) COOH Phenylalanine (C 6 H 5 ) CH 2 CH (NH 2 ) COOH Histidine (C 3 H 3 N 2 ) CH 2 CH (NH 2 ) COOH Threonine CH 3 CH (OH) CH (NH 2 ) COO Methionine CH 3 S (CH 2 )2 CH (NH 2 ) COOH Tryptophan (C 8 H 6 N) CH 2 CH (NH 2 ) COOH Nonessential Amino Acids Alanine CH 3 CH (NH 2 ) COOH Arginine H 2 NC (NH) NH (CH 2 )3 CH (NH 2 ) COOH Glycine H 2 NCH 2 COOH Proline [(CH 2 ) 3 NH CH] COOH Serine HOCH 2 CH (NH 2 ) COOH Tyrosine [C 6 H 4 (OH)] CH 2 CH (NH 2 ) COOH The injection port chamber contains dextrose with calcium. The formula for Calcium Chloride is: CaCl 2 •2H 2 O. Dextrose, USP, is chemically designated D-glucose, monohydrate (C 6 H 12 O 6 • H 2 O) and has the following structure: Dextrose is derived from corn. See Table 7 for composition, pH, osmolarity, ionic concentration and caloric content of the admixed product [see Dosage Forms and Strengths (3) ]. The dual chamber container is a lipid-compatible plastic container (PL 2401 Plastic). CLINIMIX E contains no more than 25 mcg/L of aluminum. Dextrose Hydrous Structural Formula

Uses Temporarily relieves the symptoms of the common cold including nasal and chest congestion, runny nose, sore throat, sneezing and cough.

Uses* ■ Helps temporarily relieve symptoms of common cold in children, including: ■ runny nose ■ sore throat ■ sneezing ■ cough ■ post nasal drip ■ nasal or chest congestion

INDICATIONS & USAGE SECTION Formulated for associated symptoms such as dizziness, fatigue, weakness, tingling and numb or cold extremities.

USES: Assists in relieving the symptoms of cold sores including •blistering, •dry cracked skin, •pustules, and the •pain, •burning, •itching associated with the same.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

USES: May temporary relief symptoms of cold sores and fever blisters such as: stinging - itching - swelling of minor herpatic skin eruptions of the face or genitals.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Uses this product is intended to treat symptoms of oral herpes simplex 1 or 2 after diagnosis by physician. Herpes is a viral infection. Symptoms: Rashes Blisters Redness Pain

INDICATIONS: May temporarily relieve constipation, flatulence and rumbling of colon.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Uses* See your doctor if this is the first time you have vaginal itching and discomfort to find out if you have a vaginal yeast infection. According to homeopathic indications, these ingredients provide temporary relief of yeast infection related symptoms such as: Itching and burning, occasional vaginal odor and discharge; after consultation by a physician. * These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INDICATIONS: May temporarily relieve symptoms due to acne.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INDICATIONS & USAGE SECTION Formulated for symptoms such as muscle pain, nerve pain, inflammation, joint pain and dry, shriveled skin.

USES: Temporarily relieves infrequent bowel movements, difficult passage of stool &/or other symptoms of constipation.**

Indications & Usage: Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

USES: • For the temporary relief of symptoms including: • lack of self control • anger • brain support • control of emotions • rapid thoughts • obsessive thoughts • sadness • fear These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INDICATIONS: For temporary relief of sinus congestion, dry cough in the evening and rhinitis.** **Claims based on traditional homeopathic practice, not medical evidence. Not FDA evaluated.

INDICATIONS: May temporarily relieve constriction of the chest cavity, heart sensitivity, difficulty in breathing, and swelling of the ankles.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Uses Temporarily relieves symptoms associated with sinusitus, cold, flu or allegies: -Sneezing -Nasal Stuffiness -Runny nose -Post nasal drip Removes inhaled irritants (dust, pollen) Helps to loosen thick mucous Moistens nasal passages

Uses Nasal congestion Removes inhaled irritants (dust, dirt, pollen) Moisturizes dry nasal passages

Uses Nasal congestion Removes inhaled irritants (dust, dirt, pollen) Moisturizes dry nasal passages

Uses Nasal congestion Removes inhaled irritants (dust, dirt, pollen) Moisturizes dry nasal passages

Uses Nasal congestion Removes inhaled irritants (dust, dirt, pollen) Moisturizes dry nasal passages

Uses provides instant, soothing relief to dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel and use of decongestants/steroidal sprays.

Uses Nasal congestion removes inhaled irritants- dust, dirt, pollen moisturizes dry nasal passages

Temporary relieves premenstrual symptoms such as: bloating, water retention, minor aches, lower back pain, discomfort, emotional changes, irritability

Uses: For temporary relief of minor: urinary discomfort* backache* fatigue* swelling* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INDICATIONS Teeth sensitive to cold and heat.