VAN WATERS CB-40 INSECTICIDE 10, 16, 23 & 30 OZ.
Flammability | 1 | |
Toxicity | 3 | |
Body Contact | 2 | |
Reactivity | 1 | |
Chronic | 2 | |
SCALE: Min/Nil=0 Low=1 Moderate=2 High=3 Extreme=4 |
Insecticide spray. The use of a quantity of material in an unventilated or confined space
may result in increased exposure and an irritating atmosphere developing.Before starting
consider control of exposure by mechanical ventilation. Application is by spray
atomization from a hand held aerosol pack.
Harmful by inhalation.
Irritating to eyes.
Limited evidence of a carcinogenic effect.
Dangerous for the ozone layer.
Toxic to aquatic organisms, may cause long- term adverse effects in the aquatic
environment.
Risk of explosion if heated under confinement.
Although ingestion is not thought to produce harmful effects, the material may still be damaging to the health of the individual following ingestion, especially where pre- existing organ (e.g. liver, kidney) damage is evident. Present definitions of harmful or toxic substances are generally based on doses producing mortality (death) rather than those producing morbidity (disease, ill-health). Gastrointestinal tract discomfort may produce nausea and vomiting. In an occupational setting however, ingestion of insignificant quantities is not thought to be cause for concern. Not normally a hazard due to physical form of product. Considered an unlikely route of entry in commercial/industrial environments. Ingestion may result in nausea, abdominal irritation, pain and vomiting. Ingestion of pyrethrins may produce nausea, vomiting, headache and other central nervous system disturbances. Excitation, muscular tremors and a period of shock may be followed by death. Dogs fed 5000 ppm of pyrethrum, for 90 days, developed dyspnae, tremors, ataxia and excessive salivation. An estimated fatal human dose is thought to be 100 gms. for a typical 70 kg man (1430 mg/kg).
This material can cause eye irritation and damage in some persons. Direct eye contact with petroleum hydrocarbons can be painful, and the corneal epithelium may be temporarily damaged. Aromatic species can cause irritation and excessive tear secretion.
Skin contact with the material may damage the health of the individual; systemic effects may result following absorption. The material is not thought to be a skin irritant (as classified using animal models). Temporary discomfort, however, may result from prolonged dermal exposures. Good hygiene practice requires that exposure be kept to a minimum and that suitable gloves be used in an occupational setting. Spray mist may produce discomfort. Toxic effects may result from skin absorption. The material may cause skin irritation after prolonged or repeated exposure and may produce on contact skin redness, swelling, the production of vesicles, scaling and thickening of the skin.
There is some evidence to suggest that this material, if inhaled, can irritate the throat and lungs of some persons. Inhalation of aerosols (mists, fumes), generated by the material during the course of normal handling, may be harmful. WARNING: Intentional misuse by concentrating/inhaling contents may be lethal. Anesthetics and narcotic effects (with dulling of senses and odor fatigue) are a consequence of exposure to chlorinated solvents. Individual response varies widely; odor may not be considered objectionable at levels which quickly induce central nervous system effects. High vapor concentrations may give a feeling of euphoria. This may result in reduced responses, followed by rapid onset of unconsciousness, possible respiratory arrest and death.
There has been concern that this material can cause cancer or mutations, but there is not enough data to make an assessment. There is some evidence that inhaling this product is more likely to cause a sensitization reaction in some persons compared to the general population.
Principal routes of exposure are by accidental skin and eye contact and by inhalation of vapors especially at higher temperatures. Chronic solvent inhalation exposures may result in nervous system impairment and liver and blood changes. [PATTYS]. Chronic poisoning by natural pyrethrins may result in convulsion, tetanic paralysis, rapid and uneven heart beat, liver and kidney damage, or death. The natural pyrethrins may produce hypersensitivity, especially following previous sensitising exposure. In general, repeated exposures over 2 or 3 years are required to elicit a response and involve exposure to pyrethrum rather than its individual components (including pyrethrins). The sesquiterpene lactone (pyrethrosin) and the pyrethrum glycoproteins account for the immediate and delayed hypersensitivity seen in guinea pigs following a single injection of ground chrysanthemum in Freud's adjuvant. Mild erythematic vesicular dermatitis (with papules), pruritus, localized oedema (particularly of the face, lips and eyelids), rhinitis, tachycardia, pallor and sweating are the most common syndromes. An initial skin sensitisation can progress to marked dermal oedema and skin cracking. Pyrethrum dermatitis appears to increase in hot weather or under conditions were heavy perspiration is produced. The active ingredients of pyrethrum (except pyrethrin II) are inactive in patch tests. Those patients allergic to ragweed pollen are particularly sensitive to pyrethrin. Rats fed on a diet of pyrethrins for 5000 ppm for 2 years showed some signs of tissue damage including liver lesions, bile duct proliferation and focal necrosis of the liver cells. A no-effect level of 1000 ppm found in animal experiments correspond to a daily dose of 3600 mg/man. WARNING: Aerosol containers may present pressure related hazards.