BUPROPION HYDROCHLORIDE tablet, film coated Spojené štáty - angličtina - NLM (National Library of Medicine)

bupropion hydrochloride tablet, film coated

quality care products, llc - bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - bupropion hydrochloride tablets are indicated for the treatment of major depressive disorder (mdd), as defined by the diagnostic and statistical manual (dsm). the efficacy of bupropion hydrochloride tablets in the treatment of a major depressive episode was established in two 4-week controlled inpatient trials and one 6-week controlled outpatient trial of adult subjects with mdd [see clinical studies (14)]. - bupropion hydrochloride tablets are contraindicated in patients with a seizure disorder. - bupropion hydrochloride tablets are contraindicated in patients with a current or prior diagnosis of bulimia or anorexia nervosa as a higher incidence of seizures was observed in such patients treated with bupropion hydrochloride tablets [see warnings and precautions (5.3)]. - bupropion hydrochloride tablets are contraindicated in patients undergoing abrupt discontinuation of alcohol, benzodiazepines, barbiturates, and antiepileptic drugs [see warnings and precautions (5.3) , drug interactions (7.3)].  - th

BUPROPION HYDROCHLORIDE tablet, film coated Spojené štáty - angličtina - NLM (National Library of Medicine)

bupropion hydrochloride tablet, film coated

bryant ranch prepack - bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - bupropion hydrochloride tablets are indicated for the treatment of major depressive disorder (mdd), as defined by the diagnostic and statistical manual (dsm). the efficacy of bupropion hydrochloride tablets in the treatment of a major depressive episode was established in two 4-week controlled inpatient trials and one 6-week controlled outpatient trial of adult subjects with mdd [see clinical studies (14)]. - bupropion hydrochloride tablets are contraindicated in patients with a seizure disorder. - bupropion hydrochloride tablets are contraindicated in patients with a current or prior diagnosis of bulimia or anorexia nervosa as a higher incidence of seizures was observed in such patients treated with bupropion hydrochloride tablets [see warnings and precautions (5.3)]. - bupropion hydrochloride tablets are contraindicated in patients undergoing abrupt discontinuation of alcohol, benzodiazepines, barbiturates, and antiepileptic drugs [see warnings and precautions (5.3) , drug interactions (7.3)].  - th

BUPROPION HYDROCHLORIDE tablet, film coated Spojené štáty - angličtina - NLM (National Library of Medicine)

bupropion hydrochloride tablet, film coated

aphena pharma solutions - tennessee, llc - bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - bupropion hydrochloride tablets are indicated for the treatment of major depressive disorder (mdd), as defined by the diagnostic and statistical manual (dsm). the efficacy of bupropion hydrochloride tablets in the treatment of a major depressive episode was established in two 4-week controlled inpatient trials and one 6-week controlled outpatient trial of adult subjects with mdd [see clinical studies ( 14)]. - bupropion hydrochloride tablets are contraindicated in patients with a seizure disorder.• bupropion hydrochloride tablets are contraindicated in patients with a current or prior diagnosis of bulimia or anorexia nervosa as a higher incidence of seizures was observed in such patients treated with bupropion hydrochloride tablets [ see warnings and precautions ( 5.3) ]. - bupropion hydrochloride tablets are contraindicated in patients undergoing abrupt discontinuation of alcohol, benzodiazepines, barbiturates, and antiepileptic dru

ISOTRETINOIN capsule, liquid filled Spojené štáty - angličtina - NLM (National Library of Medicine)

isotretinoin capsule, liquid filled

amneal pharmaceuticals ny llc - isotretinoin (unii: eh28up18if) (isotretinoin - unii:eh28up18if) - isotretinoin 10 mg - severe recalcitrant nodular acne isotretinoin capsules are indicated for the treatment of severe recalcitrant nodular acne. nodules are inflammatory lesions with a diameter of 5 mm or greater. the nodules may become suppurative or hemorrhagic. “severe,” by definition,2 means “many” as opposed to “few or several” nodules. because of significant adverse effects associated with its use, isotretinoin capsules should be reserved for patients with severe nodular acne who are unresponsive to conventional therapy, including systemic antibiotics . in addition, isotretinoin capsulesare indicated only for those patients who are not pregnant, because isotretinoin capsules can cause life-threatening birth defects (see boxed contraindications and warnings ). a single course of therapy for 15 to 20 weeks has been shown to result in complete and prolonged remission of disease in many patients.1,3,4 if a second course of therapy is needed, it should not be initiated until at least 8 weeks after completion of the first course, because experience has shown that patients may continue to improve while off isotretinoin capsules. the optimal interval before retreatment has not been defined for patients who have not completed skeletal growth (see warnings, skeletal, bone mineral density, hyperostosis, premature epiphyseal closure ). pregnancy: category x. see boxed contraindications and warnings . allergic reactions isotretinoin capsules are contraindicated in patients who are hypersensitive to this medication or to any of its components (see precautions, hypersensitivity ).

ULTA SPF 15 MEDIUM DEEP BROAD SPECTRUM TINTED SUNSCREEN- avobenzone, octisalate, and octocrylene lotion Spojené štáty - angličtina - NLM (National Library of Medicine)

ulta spf 15 medium deep broad spectrum tinted sunscreen- avobenzone, octisalate, and octocrylene lotion

prime enterprises, inc. - avobenzone (unii: g63qqf2nox) (avobenzone - unii:g63qqf2nox), octisalate (unii: 4x49y0596w) (octisalate - unii:4x49y0596w), octocrylene (unii: 5a68wgf6wm) (octocrylene - unii:5a68wgf6wm) - sunscreen - helps prevent sunburn - if used as directed with other sun protection measures (see directions ), decreases the risk of skin cancer and early skin aging caused by the sun

JERGENS NATURAL GLOW FACE DAILY MOISTURIZER FOR MEDIUM/TAN SKIN- avobenzone,octisalate, octocrylene lotion Spojené štáty - angličtina - NLM (National Library of Medicine)

jergens natural glow face daily moisturizer for medium/tan skin- avobenzone,octisalate, octocrylene lotion

kao usa inc. - avobenzone (unii: g63qqf2nox) (avobenzone - unii:g63qqf2nox), octisalate (unii: 4x49y0596w) (octisalate - unii:4x49y0596w), octocrylene (unii: 5a68wgf6wm) (octocrylene - unii:5a68wgf6wm) - purpose sunscreen use helps prevent sunburn do not use on damaged or broken skin stop use and ask a doctor if rash occurs

FINAFTA BABY- benzocaine liquid Spojené štáty - angličtina - NLM (National Library of Medicine)

finafta baby- benzocaine liquid

efficient laboratories inc. - benzocaine (unii: u3rsy48jw5) (benzocaine - unii:u3rsy48jw5) - purpose oral pain reliever uses for the temporary relief of sore gums due to teething in children 2 years or older

JERGENS NATURAL GLOW FACE MOISTURIZER MEDIUM TO DEEP SKIN TONES- avobenzone,octisalate, octocrylene lotion Spojené štáty - angličtina - NLM (National Library of Medicine)

jergens natural glow face moisturizer medium to deep skin tones- avobenzone,octisalate, octocrylene lotion

kao usa inc. - avobenzone (unii: g63qqf2nox) (avobenzone - unii:g63qqf2nox), octisalate (unii: 4x49y0596w) (octisalate - unii:4x49y0596w), octocrylene (unii: 5a68wgf6wm) (octocrylene - unii:5a68wgf6wm) - purpose sunscreen use helps prevent sunburn

SUN PACER SUNLESS TANNING LOTION SPF 15 Kanada - angličtina - Health Canada

sun pacer sunless tanning lotion spf 15

amway of canada, ltd. - octinoxate; ethyl salicylate; oxybenzone - lotion - 7%; 5%; 4% - octinoxate 7%; ethyl salicylate 5%; oxybenzone 4% - sunscreen agents

NEUTROGENA GLOW SUNLESS TAN.LOT SPF8-LT GLOW LOTION Kanada - angličtina - Health Canada

neutrogena glow sunless tan.lot spf8-lt glow lotion

professional pharmaceutical corp. / corp. pharmaceutique professionnelle - octinoxate - lotion - 6% - octinoxate 6% - sunscreen agents