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:  {…..}