WESTERN WATER HEMP- Western Water Hemp United States - English - NLM (National Library of Medicine)

western water hemp- western water hemp

antigen laboratories, inc. - amaranthus tuberculatus pollen (unii: 92n6w6ko2g) (amaranthus tuberculatus pollen - unii:92n6w6ko2g) - amaranthus tuberculatus pollen 0.05 g in 1 ml - allergenic extract is used for diagnostic testing and for the treatment (immunotherapy) of patients whose histories indicate that upon natural exposure to the allergen, they experience allergic symptoms. confirmation is determined by skin testing. diagnostic use of allergenic extracts usually begins with direct skin testing. this product is not intended for treatment of patients who do not manifest immediate hypersensitivity reactions to the allergenic extract following skin testing. do not administer in the presence of diseases characterized by bleeding diathesis. individuals with autoimmune disease may be at risk of exacerbating symptoms of the underlying disease, possibly due to routine immunization. patients who have experienced a recent myocardial infarction may not be tolerant of immunotherapy. children with nephrotic syndrome probably should not receive injections due to immunization causing exacerbation of nephrotic disease.

IMTRADE DEADMOUSE ZINC PHOSPHIDE BAIT Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

imtrade deadmouse zinc phosphide bait

imtrade australia pty ltd - zinc phosphide - bait - zinc phosphide ungrouped active 25.0 g/kg - vertebrate poison - agricultural or horticultural situation | canola | grain crop | legume crop | nuts | pasture | safflowers | high intensity usage - mouse - mus spp.

XEOMIN, incobotulinumtoxinA, 100  units; purified neurotoxin, free from complexing proteins Australia - English - Department of Health (Therapeutic Goods Administration)

xeomin, incobotulinumtoxina, 100 units; purified neurotoxin, free from complexing proteins

merz australia pty ltd - incobotulinumtoxina, quantity: 100 u - injection, powder for - excipient ingredients: albumin; sucrose - xeomin is indicated in adults for the treatment of:,? cervical dystonia (spasmodic torticollis),? blepharospasm,? spasticity of the upper limb,? chronic sialorrhea due to neurological disorders,? upper facial lines,- glabellar frown lines,- lateral periorbital lines (crow?s feet),- horizontal forehead lines,xeomin is indicated in children and adolescents aged 2 years to 17 years for the symptomatic treatment of:,? chronic sialorrhea due to neurological/neurodevelopmental disorders,? spasticity of the lower and/or upper limbs

XEOMIN, incobotulinumtoxinA, 50 units; purified neurotoxin, free from complexing proteins Australia - English - Department of Health (Therapeutic Goods Administration)

xeomin, incobotulinumtoxina, 50 units; purified neurotoxin, free from complexing proteins

merz australia pty ltd - incobotulinumtoxina, quantity: 50 u - injection, powder for - excipient ingredients: albumin; sucrose - xeomin is indicated in adults for the treatment of:,? cervical dystonia (spasmodic torticollis),? blepharospasm,? spasticity of the upper limb,? chronic sialorrhea due to neurological disorders,? upper facial lines,- glabellar frown lines,- lateral periorbital lines (crow?s feet),- horizontal forehead lines,xeomin is indicated in children and adolescents aged 2 years to 17 years for the symptomatic treatment of:,? chronic sialorrhea due to neurological/neurodevelopmental disorders,? spasticity of the lower and/or upper limbs

PARASITE-S- formaldehyde liquid United States - English - NLM (National Library of Medicine)

parasite-s- formaldehyde liquid

western chemical inc. - formaldehyde (unii: 1hg84l3525) (formaldehyde - unii:1hg84l3525) - formaldehyde 370 g in 1 l - 1. parasiticide for finfish: for the control of external protozoa (chilodonella spp., ichthyobodo spp., epistylis spp., ichthyophthirius spp.,ambiphrya spp. and trichodina spp.), and the monogenetic trematode parasites (cleidodiscus spp., dactylogyrus spp., and gyrodactylus spp.). 2. parasiticide for penaeld shrimp: for the control of external protozoan parasites (bodo spp., epistylis spp., and zoothamnium spp.). 3. fungicide for finflsh eggs:  for the control of fungi of the family saprolegniaceae. 4.  fungicide for freshwater-reared finfish:  for the control of mortality due to saprolegniasis associated with fungi in the family saprolegniaceae. danger poison user safety warnings  use personal protective equipment(ppe) including eye, respiratory, and skin protection while handling this product. refer to sds and osha regulations(29 cfr 1910.1048) for guidance on the most appreciate ppe equipment. failure to use ppe may increase the risk of unsafe exposure to formaldehyde. exposure to high concentrati

OVAPRIM- sgnrha and domperidone injection, solution United States - English - NLM (National Library of Medicine)

ovaprim- sgnrha and domperidone injection, solution

western chemical inc. - salmon gonadotropin releasing hormone d-arg6 analog ethyl amide acetate (unii: 66kw0e903i) (salmon gonadotropin releasing hormone d-arg6 analog ethyl amide - unii:whi058yg4q), domperidone (unii: 5587267z69) (domperidone - unii:5587267z69) - salmon gonadotropin releasing hormone d-arg6 analog ethyl amide 20 ug in 1 ml - note---in order to be legally marketed, an animal drug product intended for a minor species must be approved, conditionally approved, or indexed by the fda. this product is indexed. it is a violation of federal law to use this product in a manner other than as directed in the labeling. as used on this label, the words “ornamental fish” refer to a wide variety of finfish species maintained primarily for their appearance and do not include any fish that are consumed by humans or food-producing animals. net contents: 10 ml description: ovaprim® is a liquid peptide preparation that contains an analog of salmon gonadotropin releasing hormone (sgnrha) and a brain neurotransmitter (dopamine) inhibitor. the sgnrha in ovaprim® elicits the release of stored gonadotropins from the pituitary. the dopamine inhibitor (domperidone) serves to remove other inhibition of gnrh release. release of stored pituitary gonadotropins may aid spawning by stimulating ovulation and spermiation in sexually mature fish. indication: for

FOSTEUM- genistein, zinc glycinate citrate, and cholecalciferol capsule United States - English - NLM (National Library of Medicine)

fosteum- genistein, zinc glycinate citrate, and cholecalciferol capsule

primus pharmaceuticals, inc. - genistein (unii: dh2m523p0h) (genistein - unii:dh2m523p0h), zinc glycinate citrate (unii: h3472pj7ya) (zinc cation - unii:13s1s8sf37), cholecalciferol (unii: 1c6v77qf41) (cholecalciferol - unii:1c6v77qf41) - genistein 27 mg - each fosteum capsule contains 27 mg of genistein aglycone (genistein), derived from a natural source, for a total daily intake of 54 mg. in clinical trials, this level of intake has been shown to increase bone mineral density (bmd). genistein is chemically described as 4',5,7-trihydroxyisoflavone or 5,7-dihydroxy-3-(4-hydroxyphenyl)-4h-1-benzopyran-4-one. it is the aglycone form of the glucoside isoflavone molecule genistin. the empirical formula of genistein is c15 h10 o5 ; its molecular weight is 270.2. the structural formula is: each fosteum capsule contains 20 mg citrated zinc bisglycinate, a glycine amino acid chelate of zinc formed in the presence of citric acid that provides approximately 4 mg of elemental zinc per capsule. zinc is an essential mineral co-factor required by enzymes involved in bone metabolism and has important physiological functions in other tissues throughout the body. elemental zinc has also been shown to have synergistic effects with genistein on bone formation. this zinc bisglycin

35% PEROX-AID- hydrogen peroxide solution United States - English - NLM (National Library of Medicine)

35% perox-aid- hydrogen peroxide solution

western chemical inc. - hydrogen peroxide (unii: bbx060an9v) (hydrogen peroxide - unii:bbx060an9v) - hydrogen peroxide 350 g in 1 l - uses for freshwater-reared finfish eggs for the control of mortality in freshwater-reared finfish eggs due to saprolegniasis (fungi of the family saprolegniaceae). for freshwater-reared coldwater finfish for the control of mortality in freshwater-reared coldwater finfish (all life stages) due to saprolegniasis associated with the fungi in the family saprolegniaceae. for freshwater-reared salmonids for the control of mortality in freshwater-reared salmonids due to bacterial gill disease associated with flavobacterium branchiophilum. for the treatment and control of gyrodactylus spp. in freshwater-reared salmonids. for freshwater-reared coolwater finfish for the control of mortality in freshwater-reared coolwater finfish due to external columnaris disease associated with flavobacterium columnare. for the control of mortality in freshwater-reared coolwater finfish fingerlings and adults due to saprolegniasis associated with the fungi in the family saprolegniaceae. for freshwater-reared warmwater finfi

AQUACALM- metomidate powder United States - English - NLM (National Library of Medicine)

aquacalm- metomidate powder

western chemical inc. - metomidate (unii: z18zyl8y51) (metomidate - unii:z18zyl8y51) - metomidate 1000 mg in 1 g - indication:   for the sedation and anesthesia of ornamental finfish. aquacalmtm is not for use in fish intended for human or animal consumption. sedation may be necessary in situations such as strip spawning for hatchery rearing, transporting fish from supplier to wholesaler or retailer, photographing fish as part of a strategic marketing approach, or removal of fish from exhibit tanks prior to cleaning. anesthesia may be necessary in situations where detailed fish examination or minor surgical procedures are to be conducted.

HALAMID- chloramine-t trihydrate powder United States - English - NLM (National Library of Medicine)

halamid- chloramine-t trihydrate powder

western chemical inc. - chloramine-t trihydrate (unii: 4iu6vsv0ei) (chloramine-t anhydrous - unii:328as34ym6) - chloramine-t anhydrous 980 g in 1 kg - - before using this drug for the first time, you must inform the appropriate national pollutant discharge elimination system (npdes) permitting authority of your intentions and of the following information. a water quality benchmark for the protection of freshwater aquatic life has been derived by fda. the acute benchmark is 0.13 mg/l, which is equivalent to the secondary maximum concentration (one-half of the secondary acute value). the npdes authority may require an npdes permit before you can discharge chloramine-t. the water quality benchmark concentration is not a discharge limit, but it may be used by the npdes authority to derive one for the permit.the acute benchmark should be protective of aquatic life when the receiving water ph is at or above ph 6.5. additional environmental information on chloramine-t and the benchmark value are available in an environmental assessment posted at http://www.fda.gov/animalveterinary/developmentapprovalprocess/environmentassessments/ucm300656.htm. - before conducting