TRI OTIC- gentamicin sulfate, betamethasone valerate, and clotrimazole ointment United States - English - NLM (National Library of Medicine)

tri otic- gentamicin sulfate, betamethasone valerate, and clotrimazole ointment

med-pharmex, inc - gentamicin sulfate (unii: 8x7386qrlv) (gentamicin - unii:t6z9v48ikg), betamethasone valerate (unii: 9ifa5xm7r2) (betamethasone - unii:9842x06q6m), clotrimazole (unii: g07gz97h65) (clotrimazole - unii:g07gz97h65) - gentamicin-betamethasone-clotrimazole ointment is indicated for the treatment of canine acute and chronic otitis externa associated with yeast (malassezia pachydermatis , formerly pityrosporum canis ) and/or bacteria susceptible to gentamicin. if hypersensitivity to any of the components occurs, treatment should be discontinued and appropriate therapy instituted. concomitant use of drugs known to induce ototoxicity should be avoided. do not use in dogs with known perforation of eardrums.

SULFORAL- sulfadimethoxine oral solution solution United States - English - NLM (National Library of Medicine)

sulforal- sulfadimethoxine oral solution solution

med-pharmex, inc - sulfadimethoxine (unii: 30cpc5ldex) (sulfadimethoxine - unii:30cpc5ldex) - sulfadimethoxine 125 mg in 1 ml - indications: broiler and replacement chickens - use for the treatment of disease outbreaks of coccidiosis, fowl cholera, and infectious coryza. meat-producing turkeys - use for the treatment of disease outbreaks of coccidiosis, and fowl cholera. dairy calves, dairy heifers, and beef cattle - use for the treatment of shipping fever complex and bacterial pneumonia associated with pasteurella spp. sensitive to sulfadimethoxine; and calf diphtheria and foot rot associated with fusobacterium necrophorum (sphaerophorus necrophorus ) sensitive to sulfadimethoxine.

TETRASOL- tetracycline hydrochloride powder, for solution United States - English - NLM (National Library of Medicine)

tetrasol- tetracycline hydrochloride powder, for solution

med-pharmex, inc - tetracycline hydrochloride (unii: p6r62377kv) (tetracycline - unii:f8vb5m810t) - tetracycline hydrochloride 714 g in 1 kg - for use in the control and treatment of the following conditions in swine, calves and poultry. swine and calves indications: control and treatment of bacterial enteritis (scours) caused by escherichia   coli ; bacterial pneumonia associated with actinobacillus   pleuropneumoniae , pasteurella spp. and klebsiella spp. sensitive to tetracycline hydrochloride. recommended dosage level: use soluble powder in the drinking water at a drug level of tetracycline hydrochloride per gallon to provide 10 mg/lb of body weight per day in divided doses. caution: do not use for more than 5 consecutive days. directions for use: administer for 3-5 days. _________________________ chickens indications: control of chronic respiratory disease (crd) and air sac disease caused by mycoplasma   gallisepticum and escherichia   coli ; infectious synovitis caused by mycoplasma   synoviae sensitive to tetracycline hydrochloride. recommended dosage level: crd and air sac disease: use soluble powder in the drinking water at a drug level of 400-800 mg tetracycline hydrochloride per gallon. infectious synovitis: use soluble powder in the drinking water at a drug level of 200-400 mg tetracycline hydrochloride per gallon. _________________________ turkeys indications: control of infectious synovitis caused by mycoplasma   synoviae ; bluecomb (transmissible enteritis, coronaviral enteritis) complicated by organisms sensitive to tetracycline hydrochloride. recommended dosage level: infectious synovitis: use soluble powder in the drinking water at a drug level of 400 mg tetracycline hydrochloride per gallon. bluecomb: use soluble powder in the drinking water at a drug level of tetracycline hydrochloride per gallon to provide 25 mg/lb of body weight per day in divided doses. caution: not for use in turkeys or chickens producing eggs for human consumption. do not use for more than 14 consecutive days. directions for use: administer for 7-14 days. medicate at first clinical sign of disease or when experience indicates the disease may be a problem.

SULFASOL- sulfadimethoxine sodium powder, for solution United States - English - NLM (National Library of Medicine)

sulfasol- sulfadimethoxine sodium powder, for solution

med-pharmex, inc - sulfadimethoxine sodium (unii: 49dg2b481w) (sulfadimethoxine - unii:30cpc5ldex) - (sulfadimethoxine) antibacterial caution:federal law restricts this drug to use by or on the order of a licensed veterinarian. approved by fda under anada #200-238 each packet contains 3.34 oz. (94.6 g) sulfadimethoxine in the form of the soluble sodium salt and disodium edetate. restricted drug (california) - use only as directed.  not for human use. for broiler and replacement chickens only - use for the treatment of disease outbreaks of coccidiosis, fowl cholera, and infectious coryza. for meat-producing turkeys only - use for the treatment of disease outbreaks of coccidiosis, and fowl cholera. for dairy calves, dairy heifers, and beef cattle - use for the treatment of shipping fever complex and bacterial pneumonia associated with pasteurella spp. sensitive to sulfadimethoxine; and calf diphtheria and foot rot associated with sphaerophorus necrophorus sensitive to sulfadimethoxine. net wt.: 3.77 oz (107g)

MICONOSOL- miconazole nitrate lotion United States - English - NLM (National Library of Medicine)

miconosol- miconazole nitrate lotion

med-pharmex, inc - miconazole nitrate (unii: vw4h1cyw1k) (miconazole - unii:7nno0d7s5m) - miconosol lotion 1% and miconosol spay 1% are indicated for the treatment of fungal infections in dogs and cats caused by microsporum canis , microsporum gypseum and trichophyton mentagrophytes .

BORAX- sodium borate granule United States - English - NLM (National Library of Medicine)

borax- sodium borate granule

seroyal usa - sodium borate (unii: 91mbz8h3qo) (borate ion - unii:44oae30d22) - sodium borate 1 [hp_x] - indications for the temporary relief of motion sickness, nausea, and diarrhea indications for the temporary relief of motion sickness, nausea, and diarrhea directions adults: take five granules three times daily or as recommended by your healthcare practitioner. children: take three granules and follow adult directions.

LEVOFLOXACIN tablet, film coated United States - English - NLM (National Library of Medicine)

levofloxacin tablet, film coated

nucare pharmaceuticals,inc. - levofloxacin (unii: 6gnt3y5lmf) (levofloxacin anhydrous - unii:rix4e89y14) - levofloxacin tablets are indicated in adult patients for the treatment of nosocomial pneumonia due to methicillin-susceptible staphylococcus aureus, pseudomonas aeruginosa, serratia marcescens, escherichia coli, klebsiella pneumoniae, haemophilus influenzae, or streptococcus pneumoniae . adjunctive therapy should be used as clinically indicated. where pseudomonas aeruginosa is a documented or presumptive pathogen, combination therapy with an anti-pseudomonal β-lactam is recommended [see clinical studies (14.1)] . levofloxacin tablets are indicated in adult patients for the treatment of community-acquired pneumonia due to methicillin-susceptible staphylococcus aureus, streptococcus pneumoniae (including multi-drug-resistant streptococcus pneumoniae [mdrsp]), haemophilus influenzae, haemophilus parainfluenzae, klebsiella pneumoniae, moraxella catarrhalis, chlamydophila pn

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

naltrexone hydrochloride tablet, film coated

a-s medication solutions - naltrexone hydrochloride (unii: z6375yw9sf) (naltrexone - unii:5s6w795cqm) - naltrexone hydrochloride tablets usp 50 mg is indicated in the treatment of alcohol dependence and for the blockade of the effects of exogenously administered opioids. naltrexone hydrochloride tablets usp 50 mg has not been shown to provide any therapeutic benefit except as part of an appropriate plan of management for the addictions. naltrexone hydrochloride is contraindicated in - patients receiving opioid analgesics. - patients currently dependent on opioids, including those currently maintained on opiate agonists (e.g., methadone ) or partial agonists (e.g., buprenorphine) - patients in acute opioid withdrawal (see warnings ). - any individual who has failed the naloxone challenge test or who has a positive urine screen for opioids. - any individual with a history of sensitivity to naltrexone hydrochloride or any other components of this product.it is not known if there is any cross-sensitivity with naloxone or the phenanthrene containing opioids. naltrexone hydrochloride is a pure opioid antagonist. it does not lead to physical or psychological dependence. tolerance to the opioid antagonist effect is not known to occur.

CETAPHIL PURIFYING FACIAL BAR- triclosan soap United States - English - NLM (National Library of Medicine)

cetaphil purifying facial bar- triclosan soap

galderma laboratories, l.p. - triclosan 0.3% - antibacterial decrease bacteria on the skin

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

capstar- nitenpyram tablet

elanco us inc. - nitenpyram (unii: 3a837vz81y) (nitenpyram - unii:3a837vz81y) -