Nigeria - English - NAFDAC (National Agency for Food and Drugs Administration and Control)

menthol 17.5% cajput oil 2.5% eucalyptus oil 75%, peppermint oil 0.2%

Nigeria - English - NAFDAC (National Agency for Food and Drugs Administration and Control)

menthol 7.5%,cajuput oil 2.5%,lavender oil 8.0%,peppermint oil 0.2%,eucalyptus oil 7.5%

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

axichem pty ltd - haloxyfop present as haloxyfop-p methyl ester - emulsifiable concentrate - haloxyfop present as haloxyfop-p methyl ester phenoxy acids-ester active 520.0 g/l - herbicide - apple | avocado | banana | blueberry | canola | chickpea | citrus | clover pasture | clover seed crop | cotton | cowpea | custar - annual ryegrass | barley grass | barnyard grass or water grass | barnyard or water grass | brome grass | buffel grass | common storksbill | couch | crowsfoot grass | english couch or rope twitch | erodium spp. | green panic | johnson grass | johnson grass - rhizome | johnson grass - seedling | kikuyu grass | lesser canary grass | liverseed grass - seedling | liverseed or urochloa grass | long storksbill, corkscrew | mossman river or burr grass | musky crowfoot | native millet | paradoxa grass | paspalum spp. | pigeon grass | prairie grass | rat's tail grasses | rhodes grass | summer grass | volunteer cereal | wild oat | abyssinian rhodes grass | agropyron repens | annual canary grass | annual phalaris | australian millet | barnyard grass | blowaway grass | bromus diandrus | bromus rigidus | canary grass | common crowsfoot | crab grass | dropseed grass | ferny leaf storksbill | giant parramatta grass | liverseed grass | mossman burr grass | musky storksbill | parramatta grass | pigeon weed | purple pigeon gras

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

organon pharma pty ltd - ezetimibe, quantity: 10 mg - tablet - excipient ingredients: povidone; magnesium stearate; microcrystalline cellulose; sodium lauryl sulfate; croscarmellose sodium; lactose monohydrate - adults ( greater than or equal to 18 years) primary hypercholesterolaemia ezetrol administered alone, or with an hmg-coa reductase inhibitor (statin), is indicated as adjunctive therapy to diet in patients with primary (heterozygous familial and non-familial) hypercholesterolaemia.,homozygous familial hypercholesterolaemia (hofh) ezetrol, administered with a statin, is indicated for patients with hofh. patients may also receive adjunctive treatments (e.g., ldl apheresis).,homozygous sitosterolaemia (phytosterolaemia) ezetrol is indicated for the reduction of elevated sitosterol and campesterol levels in patients with homozygous familial sitosterolaemia.,prevention of cardiovascular disease ezetrol, is indicated for administration in combination with the maximum tolerated dose of a statin with proven cardiovascular benefit in patients with coronary heart disease (chd) and a history of acute coronary syndrome (acs) in need of additional lowering of ldl-c in the expectation of a modest further reduction in the r

Israel - English - Ministry of Health

organon pharma israel ltd., israel - ezetimibe - tablets - ezetimibe 10 mg - ezetimibe - ezetimibe - primary hypercholesterolemia: ezetrol administered with an hmg-coa reductase inhibitor (statin) or alone are indicated as adjunctive therapy to diet for use in patients with primary (heterozygous familial and non-familial) hypercholesterolemia. homozygous familial hypercholesterolemia (hofh): ezetrol administered with a statin are indicated for use in patients with hofh.patients may also receive adjunctive treatments (e.g. ldl apheresis).homozygous sitosterolemia (phytosterolemia): ezetrol are indicated for use in patients with homozygous familial sitosterolemia.

Malaysia - English - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

organon malaysia sdn. bhd. - ezetimibe -

Malaysia - English - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

organon malaysia sdn. bhd. - ezetimibe -

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

merck sharp & dohme australia pty ltd - ezetimibe -

New Zealand - English - Medsafe (Medicines Safety Authority)

merck sharp & dohme (new zealand) limited - ezetimibe 10mg - tablet - 10 mg - active: ezetimibe 10mg excipient: croscarmellose sodium lactose monohydrate magnesium stearate microcrystalline cellulose povidone purified water sodium laurilsulfate

Ireland - English - HPRA (Health Products Regulatory Authority)

ltt pharma limited - ezetimibe - tablets - 10 milligram - other lipid modifying agents