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

salsalate tablet

caraco pharmaceutical laboratories, ltd. - salsalate (unii: v9mo595c9i) (salsalate - unii:v9mo595c9i) - salsalate 500 mg - carefully consider the potential benefits and risks of salsalate tablets, usp and other treatment options before deciding to use salsalate tablets, usp. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings ). salsalate is indicated for relief of the signs and symptoms of rheumatoid arthritis, osteoarthritis and related rheumatic disorder. salsalate tablet, usp is contraindicated in patients with known hypersensitivity to salsalate. salsalate tablet, usp should not be given to patients who have experienced asthma, urticaria, or allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients (see warnings - anaphylactoid reactions , and precautions - preexisting asthma ). salsalate tablet, usp is contraindicated for the treatment of peri-operative pain in the setting of coronary artery bypass graft (cabg) surgery (see warnings ). drug abuse and depen

NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION-  hydroquinone, octinoxate,and zinc oxide kit United States - English - NLM (National Library of Medicine)

nu-derm system normal-dry skin transformation- hydroquinone, octinoxate,and zinc oxide kit

omp, inc. - hydroquinone (unii: xv74c1n1ae) (hydroquinone - unii:xv74c1n1ae) - hydroquinone 40 mg in 1 g - the gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines, and other unwanted areas of melanin hyperpigmentation. the gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines, and other unwanted areas of melanin hyperpigmentation. specially formulated for blending purposes as part of the obagi nu-derm system. - 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

ICE SUN BC AIR PUFF- titanium dioxide, octinoxate, zinc oxide, octisalate liquid United States - English - NLM (National Library of Medicine)

ice sun bc air puff- titanium dioxide, octinoxate, zinc oxide, octisalate liquid

popco co.,ltd. - titanium dioxide (2.8%), octinoxate (ethylhexyl methoxycinnamate) (2.1%), zinc oxide (1.6%), octisalate (ethylhexyl salicylate) (1.4%) - sunscreen helps prevent sunburn

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

glyburide tablet

trupharma, llc - glyburide (unii: sx6k58tvwc) (glyburide - unii:sx6k58tvwc) - glyburide 2.5 mg - glyburide tablets usp are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. glyburide tablets are contraindicated in patients with: - known hypersensitivity or allergy to the drug. - diabetic ketoacidosis, with or without coma. this condition should be treated with insulin. - type i diabetes mellitus. - concomitant administration of bosentan.

DICLOFENAC SODIUM DELAYED RELEASE- diclofenac sodium tablet, delayed release United States - English - NLM (National Library of Medicine)

diclofenac sodium delayed release- diclofenac sodium tablet, delayed release

carlsbad technology, inc. - diclofenac sodium (unii: qtg126297q) (diclofenac - unii:144o8ql0l1) - diclofenac sodium 50 mg - carefully consider the potential benefits and risks of diclofenac sodium delayed-release tablets and other treatment options before deciding to use diclofenac. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals ( see warnings; gastrointestinal bleeding, ulceration, and perforation ). diclofenac is 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 takin

NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION- hydroquinone, octinoxate, and zinc oxide kit United States - English - NLM (National Library of Medicine)

nu-derm system normal-dry skin transformation- hydroquinone, octinoxate, and zinc oxide kit

omp, inc. - octinoxate 7.5% zinc oxide 10.5% - the gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines, and other unwanted areas of melanin hyperpigmentation. the gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines, and other unwanted areas of melanin hyperpigmentation. specially formulated for blending purposes as part of the obagi nu-derm system. 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

METFORMIN HYDROCHLORIDE tablet, coated United States - English - NLM (National Library of Medicine)

metformin hydrochloride tablet, coated

megalith pharmaceuticals inc - metformin hydrochloride (unii: 786z46389e) (metformin - unii:9100l32l2n) - metformin hydrochloride 500 mg - metformin hydrochloride tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults and children with type 2 diabetes mellitus. metformin hydrochloride tablets are contraindicated in patients with: - severe renal impairment (egfr below 30 ml/min/1.73 m 2 ) (see  warnings and precautions ). - known hypersensitivity to metformin hydrochloride. - acute or chronic metabolic acidosis, including diabetic ketoacidosis, with or without coma. diabetic ketoacidosis should be treated with insulin. 

BISMUTH SUBSALICYLATE/METRONIDAZOLE/TETRACYCLINE HYDROCHLORIDE- bismuth subsalicylate chewable tablets/metronidazole tablets/tet United States - English - NLM (National Library of Medicine)

bismuth subsalicylate/metronidazole/tetracycline hydrochloride- bismuth subsalicylate chewable tablets/metronidazole tablets/tet

ailex pharmaceuticals, llc - bismuth subsalicylate (unii: 62tey51rr1) (salicylic acid - unii:o414pz4lpz) - the components of bismuth subsalicylate chewable tablets/ metronidazole tablets/tetracycline hydrochloride capsules (bismuth subsalicylate, metronidazole, and tetracycline hydrochloride), in combination with an h2 antagonist, are indicated for the eradication of h. pylori for treatment of patients with h. pylori infection and duodenal ulcer disease (active or a history of duodenal ulcer). the eradication of h. pylori has been demonstrated to reduce the risk of duodenal ulcer recurrence in patients with active duodenal ulcer disease (see clinical studies and dosage and administration ). to reduce the development of drug-resistant bacteria and maintain the effectiveness of bismuth subsalicylate chewable tablets/metronidazole tablets/tetracycline hydrochloride capsules and other antibacterial drugs, bismuth subsalicylate chewable tablets/metronidazole tablets/tetracycline hydrochloride capsules should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptib

GREEN TEA GEL HAND SANITIZER- ethanol 75% gel United States - English - NLM (National Library of Medicine)

green tea gel hand sanitizer- ethanol 75% gel

mingshi technology co., ltd - alcohol (unii: 3k9958v90m) (alcohol - unii:3k9958v90m) - antiseptic to help reduce bacteria on the skin, when soap and water are not available do not use with children less than 2 months of age supervise children under 6 years of age when using this product to avoid swallowing or getting in eyes and on face do not use on open wounds or broken skin. stop use and ask a doctor if irritation or rash occurs. these may be signs of a serious condition

COLOGNAID HAND SANITIZING GREEN TEA- alcohol spray United States - English - NLM (National Library of Medicine)

colognaid hand sanitizing green tea- alcohol spray

narem kozmetik urunleri ve bilisim sanayi ticaret limited sirketi - alcohol (unii: 3k9958v90m) (alcohol - unii:3k9958v90m) - antiseptic for hand sanitizing, keeps your hands clean and refreshed. recommended for repeated use. rinse free