Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

smiths medical asd, inc. - povidone-iodine (unii: 85h0hzu99m) (iodine - unii:9679tc07x4) - povidone-iodine 0.10 mg in 1 ml - indications and usage sodium chloride injection is used to flush intravascular catheters or as a sterile, isontonic single dose vehicle, solvent, or diluent for substances to administered intravenously,k intramuscularly or sub-cutaneously and for other extemporaneously prepared single dose sterile solutions according to instructions of the manufacture of the drug to be administered.

Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

smiths medical asd, inc. - povidone-iodine (unii: 85h0hzu99m) (iodine - unii:9679tc07x4) - povidone-iodine 0.10 mg in 1 ml - indications and usage sodium chloride injection is used to flush intravascular catheters or as a sterile, isontonic single dose vehicle, solvent, or diluent for substances to administered intravenously,k intramuscularly or sub-cutaneously and for other extemporaneously prepared single dose sterile solutions according to instructions of the manufacture of the drug to be administered.

Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

smiths medical asd, inc. - povidone-iodine (unii: 85h0hzu99m) (iodine - unii:9679tc07x4) - povidone-iodine 0.10 mg in 1 ml - indications and usage sodium chloride injection is used to flush intravascular catheters or as a sterile, isontonic single dose vehicle, solvent, or diluent for substances to administered intravenously,k intramuscularly or sub-cutaneously and for other extemporaneously prepared single dose sterile solutions according to instructions of the manufacture of the drug to be administered.

Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

smiths medical asd, inc. - povidone-iodine (unii: 85h0hzu99m) (iodine - unii:9679tc07x4) - povidone-iodine 0.10 ml in 1 ml - indications and usage sodium chloride injection is used to flush intravascular catheters or as a sterile, isontonic single dose vehicle, solvent, or diluent for substances to administered intravenously,k intramuscularly or sub-cutaneously and for other extemporaneously prepared single dose sterile solutions according to instructions of the manufacture of the drug to be administered.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

novartis pharmaceuticals australia pty ltd - ciprofloxacin hydrochloride, quantity: 3.5 mg/ml (equivalent: ciprofloxacin, qty 3 mg/ml) - ear drops, solution - excipient ingredients: purified water; sodium acetate; mannitol; hydrochloric acid; glacial acetic acid; benzalkonium chloride; disodium edetate; sodium hydroxide - treatment of chronic suppurative otitis media caused by organisms susceptible to ciprofloxacin in adults and children one month of age or older.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

novartis pharmaceuticals australia pty ltd - ciprofloxacin hydrochloride, quantity: 3.5 mg/ml (equivalent: ciprofloxacin, qty 3 mg/ml) - ear drops, solution - excipient ingredients: mannitol; purified water; benzalkonium chloride; sodium hydroxide; disodium edetate; sodium acetate; hydrochloric acid; glacial acetic acid - treatment of chronic suppurative otitis media caused by organisms susceptible to ciprofloxacin in adults and children one month of age or older.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

sanofi-aventis healthcare pty ltd t/a sanofi consumer healthcare - tramazoline hydrochloride, quantity: 1.184 mg/ml - spray, solution - excipient ingredients: purified water; glycerol; sodium chloride; hypromellose; sodium bicarbonate; magnesium sulfate heptahydrate; magnesium chloride hexahydrate; sodium hydroxide; camphor; cineole; povidone; calcium chloride dihydrate; benzalkonium chloride; menthol; citric acid monohydrate - for the symptomatic relief of nasal congestion associated with common cold, hayfever and rhinitis.

Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

nucare pharmaceuticals,inc. - povidone-iodine (unii: 85h0hzu99m) (iodine - unii:9679tc07x4) - lidocaine hydrochloride injection, usp is indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks, when the accepted procedures for these techniques as described in standard textbooks are observed. lidocaine hydrochloride is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.  bupivacaine hydrochloride injection, usp is not recommended for intravenous regional anesthesia (bier block). see warnings. the routes of administration and indicated bupivacaine hydrochloride injection, usp concentrations are: local infiltration 0.25% peripheral nerve block 0.25% and 0.5% retrobulbar block 0.75% sympathetic block 0.25% lumbar epidural 0.25%, 0.5%, and 0.75% (0.75% not for obstetrical anesthesi

Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

rx pharma-pack, inc. - lidocaine hydrochloride anhydrous (unii: ec2cnf7xfp) (lidocaine - unii:98pi200987) - lidocaine hydrochloride anhydrous 10 mg in 1 ml - lidocaine hcl is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type. sodium chloride injection, usp, 0.9% preparations are indicated for diluting or dissolving drugs for intramuscular, intravenous or subcutaneous injection according to instructions of the manufacturer of the drug to be administered. sodium chloride injection, usp, 0.9% is also indicated for use in flushing of intravenous catheters. antiseptic antiseptic skin preparation antiseptic for preparation of the skin prior to injection.

Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

tender corporation dba adventure medical kits - active ingredient: .........bacitracin zinc 400 units, neomycin sulfate 5mg ( equivalent to 3.5 mg neomycin base), polymyxin b sulfate 5000 units - for professional and hospital use.  helps prevent infection.  antiseptic cleansing of face, hands and body without soap and water. stop use if unusual redness, swelling or other symptoms occur. consult a physician immediately. do not use in the eyes or over large areas of the body. triple antibiotic uses:  to help prevent infection in: minor cuts;  scrapes;  burns do not use:  in eyes;  over large areas of the body; if allergic to any of the ingredients;  for more than one week unless directed by a physician. stop use and consult a doctor: if the condition persists or gets worse;  a rash or other allergic reaction develops pain reliever/fever reducer temporarily relieves minor aches and pains associated with - headache - minor arthritis - common cold - menstrual cramps - muscular aches - backache - toothache temporarily reduces fever. antihistamine temporarily relieves runny nose and decreases sneezing, itching of the nose and throat, itchy-watery eyes due to hay fever or other respiratory allergies. purpos