Australia - English - Department of Health (Therapeutic Goods Administration)

novapharm research (australia) pty ltd - iodine, quantity: 0.75 % w/w - liquid, multipurpose - excipient ingredients: purified water; phenoxyethanol; phosphoric acid; propan-1-ol; sodium nitrite; hyetellose; glycerol; povidone; potassium iodide; propylene glycol; ethanol; sodium chloride; cocamidopropyl betaine; fragrance (perfume) - antiseptic, surgical scrub

Australia - English - Department of Health (Therapeutic Goods Administration)

novapharm research (australia) pty ltd - iodine, quantity: 1 % w/w - solution - excipient ingredients: phenoxyethanol; phosphoric acid; purified water; propylene glycol; sodium nitrite; povidone; ethanol; potassium iodide; sodium chloride; cocamidopropyl betaine - for antisepsis of minor cuts and abrasions and treatment of minor skin infections.

Australia - English - Department of Health (Therapeutic Goods Administration)

novapharm research (australia) pty ltd - iodine, quantity: 0.75 % w/w - liquid, multipurpose - excipient ingredients: potassium iodide; ethanol; povidone; phenoxyethanol; purified water; sodium nitrite; propan-1-ol; phosphoric acid; propylene glycol; hyetellose; glycerol; sodium chloride; cocamidopropyl betaine - antiseptic, surgical scrub

Australia - English - 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.

Australia - English - 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.

Australia - English - 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.

United States - English - NLM (National Library of Medicine)

smiths medical asd, inc. - povidone-iodine (unii: 85h0hzu99m) (iodine - unii:9679tc07x4) - povidone-iodine 0.10 mg in 1 ml - 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 is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type. 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. lidocaine hydrochloride and epinephrine injection, usp is indicated

United States - English - NLM (National Library of Medicine)

smiths medical asd, inc. - povidone-iodine (unii: 85h0hzu99m) (iodine - unii:9679tc07x4) - povidone-iodine 0.10 mg in 1 ml - 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 is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type. 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.

United States - English - 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. lidocaine hydrochloride and epinephrine injection, usp is indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection, 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 is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.

United States - English - NLM (National Library of Medicine)

smiths medical asd, inc. - povidone-iodine (unii: 85h0hzu99m) (iodine - unii:9679tc07x4) - povidone-iodine 0.10 mg in 1 ml - lidocaine hydrochloride and epinephrine injection, usp is indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection, 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 is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type. bupivacaine hydrochloride is indicated for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and for obstetrical procedures. only the 0.25% and 0.5% concentrations are indicated for obstetrical anesthesia. (see warnings .) experience with nonobstetrical surgical procedures in pregnant patients is not sufficient to recommend use of 0.75% concentration of bupivacaine hydrochlo