The acute oral toxicity of {test material} to X-d-old {common name and scientific name} was assessed over days in accordance with the . {specify the guideline followed}. {Test material was administered to the birds {enter the number of birds per treatment} by {method} at {Indicate doses used} mg ai/kg bw. The day-acute oral LD50 was mg ai/kg bw. The day NOEL of {test material} to the {species}, based on {endpoint} was mg ai/kg bw. According to the US EPA classification, {test material} would be classified as [toxicity classification] to {species} on an acute oral basis.


[Describe toxicity briefly including mortality, behavioral abnormalities, and other signs of toxicity. If there was no toxicity, state that there was no compound related toxicity effect.]


This toxicity study is classified as {acceptability classification e.g.

Acceptable/unacceptable/supplementary} and {satisfies/does not satisfy} the guideline requirement for [indicate study type and species].


Results Synopsis


Test Organism Size/Age (mean weight):


LD50: {. Mg a.i./kg bw} 95% C.I.: { to mg a.i./kg bw}

NOEL: { mg a.i./kg bw} Probit Slope: {..}

Endpoint(s) Effected: {..}