DICLOFENAC SODIUM tablet, delayed release Estados Unidos - inglés - NLM (National Library of Medicine)

diclofenac sodium tablet, delayed release

advagen pharma ltd - diclofenac sodium (unii: qtg126297q) (diclofenac - unii:144o8ql0l1) - carefully consider the potential benefits and risks of diclofenac sodium delayed-release tablets and other treatment options before deciding to use diclofenac sodium. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings; gastrointestinal bleeding, ulceration, and perforation). diclofenac sodium delayed-release tablets are indicated: • for relief of the signs and symptoms of osteoarthritis • for relief of the signs and symptoms of rheumatoid arthritis • for acute or long-term use in the relief of signs and symptoms of ankylosing spondylitis diclofenac sodium delayed-release tablets are contraindicated in the following patients: • known hypersensitivity (e.g., anaphylactic reactions and serious skin reactions) to diclofenac or any components of the drug product (see warnings; anaphylactic reactions, serious skin reactions). • history of asthma, urticaria, or other allergic-type reactions after taking aspirin or other nsaid

EYECON Israel - inglés - Ministry of Health

eyecon

gem pharma ltd - hyaluronic acid as sodium - eye drops, solution - hyaluronic acid as sodium 0.15 mg/ml - hyaluronic acid - hyaluronic acid - symptomatic treatment of dry eye syndrome.

PHARMACY ACTION PARACETAMOL & IBUPROFEN film coated tablet blister pack Australia - inglés - Department of Health (Therapeutic Goods Administration)

pharmacy action paracetamol & ibuprofen film coated tablet blister pack

generic health pty ltd - ibuprofen, quantity: 200 mg; paracetamol, quantity: 500 mg - tablet, film coated - excipient ingredients: hypromellose; crospovidone; pregelatinised maize starch; titanium dioxide; microcrystalline cellulose; colloidal anhydrous silica; purified talc; magnesium stearate; povidone; purified water; polysorbate 80; polyvinyl alcohol; macrogol 3350; mica - temporary relief of acute (short term) pain and / or inflammation associated with headache, migraine headache, tension headache, sinus pain, toothache, dental procedures, backache, muscular aches and pains, period pain, sore throat, tennis elbow, rheumatic pain and arthritis, and the aches and pains associated with colds and flu. reduces fever.

PHARMACY ACTION HAYFEVER & SINUS  PAIN RELIEF PSE tablet blister pack Australia - inglés - Department of Health (Therapeutic Goods Administration)

pharmacy action hayfever & sinus pain relief pse tablet blister pack

noumed pharmaceuticals pty ltd - pseudoephedrine hydrochloride, quantity: 30 mg; chlorphenamine maleate, quantity: 2 mg; paracetamol, quantity: 500.4 mg - tablet, uncoated - excipient ingredients: microcrystalline cellulose; magnesium stearate; crospovidone; pregelatinised maize starch; povidone; purified water; erythrosine aluminium lake; stearic acid - temporary relief of the symptoms of sinus headache, pain and nasal congestion (including fever) and hay fever.

LITTLES VAPOR RUB- camphor, eucalyptus oil, menthol ointment Estados Unidos - inglés - NLM (National Library of Medicine)

littles vapor rub- camphor, eucalyptus oil, menthol ointment

littles skin care, inc - camphor (natural) (unii: n20hl7q941) (camphor (natural) - unii:n20hl7q941), eucalyptus oil (unii: 2r04oni662) (eucalyptus oil - unii:2r04oni662), menthol (unii: l7t10eip3a) (menthol - unii:l7t10eip3a) - rub gently on chest. apply at the bottom of feet. apply on chest and under the feet. temporarily relieves cough and congestion.

LITTLES ALL NATURAL ARTHRITIC PAIN RELIEF- capsacin ointment Estados Unidos - inglés - NLM (National Library of Medicine)

littles all natural arthritic pain relief- capsacin ointment

littles skin care, inc. - capsaicin (unii: s07o44r1zm) (capsaicin - unii:s07o44r1zm), menthol (unii: l7t10eip3a) (menthol - unii:l7t10eip3a) - temporarily helps relieve sore muscles and joint pain (arthritic) pain. massage the painful area until thoroughly absorbed. wash hands thorougly after use. if burning sensation occurs, stop its use. wash the area with soap and water or with vinegar and then with soap and water. you may use a glove for applying. if burning sensation occurs, stop its use. wash the area with soap and water or with vinegar and then with soap and water. massage the painful area until thoroughly absorbed.. apply twice a day.

CEFUROXIME MARTINDALE PHARMA Irlanda - inglés - HPRA (Health Products Regulatory Authority)

cefuroxime martindale pharma

martindale pharmaceuticals ltd - cefuroxime sodium - pdr for soln for injection - 750 base milligrams