Hydroquinone Test Results
Proposed Test Rule/Test Standards (PRM)
50 FR 53160; December 30, 1985
Final Test Rule/Test Standards (FRM)
52 FR 19865; May 28, 1987
Chemical Manufacturer's Association (CMA) Hydroquinone Program Panel (HPP)
54 FR 27353; June 29, 1989/Test standards
Project Manager: D. Price, R. Locke
Section Chief: R. Troast
Status: Closed. All required tests have been completed. Test results have been forwarded to the Risk Assessment Division for review and disposition.Announced Receipt of Test Data
Eastman Kodak submitted: developmental toxicity study (rats); metabolic fate study in male and female rats and percutaneous absorption study (beagle dogs) (51 FR 6468; February 24, 1986). The last two studies were part of a voluntary testing program.
Eastman Kodak submitted a blood elimination kinetic study with hydroquinone being administered by intragastric intubation, intratracheal instillation, or intravenous injection to male rats (51 FR 16203; May 1, 1986). This submission was part of a voluntary testing program.
The CMA's HPP submitted a toxicokinetic study in male and female rats (53 FR 28909; August 1, 1988) and a subchronic oral toxicity study (rats) using a functional observational battery and neuropathology to detect neurotoxicity (53 FR 47867; November 28, 1988).
CMA's HPP submitted a 2-generation reproduction study (rats) (55 FR 357; January 4, 1990).