Fido's Grooming MSDS 84-FP5100_5120_5130 - Fre-Itch Rinse Concentrate | Page 9

Chemwatch: 34-9443 Page 9 of 12 Version No: 4.1.1.1 Issue Date: 02/13/2014 Fido's Fre-Itch Rinse Concentrate For Dogs, Cats, Puppies, Kittens And Cage Birds Print Date: 06/27/2016 absorbed doses high enough to significantly affect the mixed function oxidase enzymes would be required. It is unlikely that these levels would occur based on the registered uses of pyrethrins. Neurotoxicity: There is a concern for neurotoxicity resulting from exposure to pyrethrins, based on tremors in female rats, decreased motor activity in male rats, and neuropathology in both sexes in a rat acute neurotoxicity study; clinical signs (excessive salivation and head arched backward) in a female rabbit following exposure during gestation; and tremors in female rats in a subchronic inhalation study. In the range-finding developmental toxicity studies in rats and rabbits, tremors/convulsions were observed in those that died during the study. In the mouse 90-day range-finding study, tremors and increased/decreased activity were observed at dose levels that also resulted in mortality. Pyrethrins are axonic poisons. Reproductive toxicity: In the two generation rat reproduction study, parental male systemic and reproductive toxicity were detected at 1000 ppm (65 mg/kg body weight per day) and parental female systemic toxicity was detected at 3000 ppm (196 mg/kg body weight per day). The NOAEL for parental systemic (male) and reproductive toxicity was 100 ppm (6.4 mg/kg body weight-day). Cancer: Pyrethrins are classified as “Suggestive Evidence of Carcinogenicity, but Not Sufficient to Assess Human Carcinogenic Potential,” based on the weight-of-the-evidence including the occurrence of benign liver tumors in female rats, no treatment-related increase in liver tumors in male rats, no treatment-related increase in tumors in either sex of mice, and no concern for mutagenicity. Endocrine disruption: There is evidence that pyrethrins are associated with endocrine disruption. Direct measurements of serum thyroid hormones [T3, T4, and TSH], as well as histopathological alterations in the thyroid (i.e. follicular cell hypertrophy, follicular cell hyperplasia, follicular cell adenomas and/or carcinomas) indicate there is concern regarding the potential for endocrine disruption When the appropriate screening and/or testing protocols have been developed, pyrethrins may be subject to additional screening and/or testing. Pyrethrins and pyrethroids: Pyrethrins are botanical insecticides that come from the pyrethrum flower, Chrysanthemum cinerariaefolium. Pyrethrins have limitations because of the cost of production and instability in sunlight; therefore, many synthetic pyrethrins-like compounds were developed to be more stable in sunlight and cost effective. These compounds are referred to as synthetic pyrethroids. Although all pyrethroids interact with sodium channels, there are multiple types of sodium channels and it is currently unknown whether the pyrethrins and pyrethroids have similar effects on all channels NOTE: Studies with rats and mice indicate rapid oxidation of pyrethrin I. Within 48 hrs. metabolites appear in urine (46%) and in expired CO2 (0.3%) (1). Some unmetabolised substance is found in faeces (2). The synergist, piperonyl butoxide, does not enhance the acute toxicity of the substance (1). Hutson D.H; Progress in Drug Metabolism 3:215-252 1979 (2). Hayes W.J.; Pesticide Studies in Man William Wilkins pp 75-80 WATER No significant acute toxicological data identified in literature search. Acute Toxicity Carcinogenicity Skin Irritation/Corrosion Reproductivity Serious Eye Damage/Irritation STOT - Single Exposure Respiratory or Skin sensitisation STOT - Repeated Exposure Mutagenicity Aspiration Hazard Legend: – Data available but does not fill the criteria for classification – Data required to make classification available – Data Not Available to make classification SECTION 12 ECOLOGICAL INFORMATION Toxicity Ingredient Endpoint Test Duration (hr) Species Value Source 2-ethylhexyl bicycloheptene dicarboximide EC50 48 Crustacea 2.3mg/L 4 2-ethylhexyl bicycloheptene dicarboximide LC50 96 Fish 1.4mg/L 4 piperonyl butoxide EC50 48 Crustacea 0.1mg/L 4 piperonyl butoxide LC50 96 Fish 0.0024mg/L 4 piperonyl butoxide NOEC 48 Crustacea 0.01mg/L 4 piperonyl butoxide EC50 96 Crustacea 0.23mg/L 2 piperonyl butoxide EC50 72 Algae or other aquatic plants 0.85mg/L 2 pyrethrin I EC50 96 Algae or other aquatic plants 0.024mg/L 3