In an acute dermal toxicity study (MRID [number]), groups of (young adult) (strain) (species - rats or rabbits) (#/sex) were dermally exposed to chemical name (% a.i) in (name of vehicle if appropriate) for [#] hours to (% or amount of body surface area) at doses of x, x, or x mg/kg bw. Animals then were observed for [#] days.
Dermal LD50 Males = mg/kg bw (95% C.I. if available)
Females = mg/kg bw (95% C.I. if available)
Combined = mg/kg bw (95% C.I. if available)
(or note if no mortality occurred, note if limit test)
(Chemical name) is of (LOW, SLIGHT, MODERATE, HIGH) Toxicity based on (males or females which ever is lower) [include EPA Toxicity Category I, II, III or IV if joint review]. Label comment if applicable.
(Include only major treatment related dermal, clinical signs, body weight or necropsy signs including onset and/or duration if any, or the following statement: There were no treatment related clinical signs, necropsy findings or changes in body weight.) Note if there was a NOAEL for clinical findings (for Acute reference dose consideration during subsequent risk assessment.)