New Zealand - English - Medsafe (Medicines Safety Authority)

sanofi-aventis new zealand limited - benzocaine 1.4%{relative}; chlorobutanol 1%{relative}; ephedrine hydrochloride 1%{relative}; glycerol; phenazone 5.5%{relative}; potassium hydroxyquinoline sulfate 0.1%{relative} - ear drops - 1.4/1/1/qs/5.5/0.1% - active: benzocaine 1.4%{relative} chlorobutanol 1%{relative} ephedrine hydrochloride 1%{relative} glycerol phenazone 5.5%{relative} potassium hydroxyquinoline sulfate 0.1%{relative}

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

ecolab healthcare division - potassium hydroxyquinoline sulfate; hydrocortisone - cutaneous cream - 5mg/1gram ; 10mg/1gram

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

coopersurgical, inc. - oxyquinoline sulfate (unii: 61vug75y3p) (oxyquinoline - unii:5utx5635hp), sodium lauryl sulfate (unii: 368gb5141j) (lauryl sulfate - unii:diq16uc154) - 1. to help restore and maintain normal vaginal acidity. 2.   to coat walls of vagina with a lubricating film that may help reduce odor-causing bacteria, since bacteria can flourish in abnormal vaginal ph. 1. unscrew cap from tube 2. pierce end of tube with top of cap (a small amount of trimo-san may escape when top of tube is pierced). 3. attach threaded end of the universal applicator to trimo-san tube (see picture 1). 4. while holding the universal applicator, squeeze the tube from the bottom until trimo-san reaches the specified dosage level (see picture 2). 5. detach the universal applicator from the tube. gently insert the universal applicator approximately ½ inch into the vagina.     press in the plunger of the universal applicator to dispense the gel. keep the plunger pressed until the universal applicator is removed from the vagina. note: for those wearing an inflat-o-ball or cube pessary, remove pessary per physician’s instruction before application of trimo-san. 6. clean the universal applic

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

denison pharmaceuticals, llc - oxyquinoline sulfate (unii: 61vug75y3p) (oxyquinoline - unii:5utx5635hp), sodium lauryl sulfate (unii: 368gb5141j) (lauryl sulfate - unii:diq16uc154) -

Namibia - English - Namibia Medicines Regulatory Council

novartis south africa (pty) ltd - 8-hydroxyquinoline - ointment - 8-hydroxyquinoline

Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

cmc chemicals pty limited - 8-hydroxyquinoline - granular formulation - 8-hydroxyquinoline quinoline active 1.0 g/kg - fungicide - grapevine graft - parent stock - botrytis | botrytis blight | bunch rot-grey mould | grey mould | grey mould (nesting) | storage rot

New Zealand - English - Medsafe (Medicines Safety Authority)

pfizer new zealand limited - diiodohydroxyquinoline 100mg - pessary - 100 mg - active: diiodohydroxyquinoline 100mg

Canada - English - Health Canada

vermonts original llc - oxyquinoline sulfate - ointment - 0.3% - oxyquinoline sulfate 0.3% - mercury, metallic - cattle

Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

bayer cropscience pty ltd - hydroxyquinoline sulfate - fungicide - box, case - preventative spray | grapevine graft - parent stock - grey mould - botrytis cinerea | botrytis blight | botrytis rot | bunch rot

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

proqualix pty ltd - in administration - diiodohydroxyquinoline, quantity: 102.6 mg - pessary - excipient ingredients: lactose monohydrate; glucose; acacia; dextrin; maize starch; sodium thiosulfate pentahydrate; phosphoric acid; purified talc; magnesium stearate