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  2. Toxicity label - Wikipedia

    en.wikipedia.org/wiki/Toxicity_label

    Toxicity labels [1] viz; red label, yellow label, blue label and green label are mandatory labels employed on pesticide containers in India identifying the level of toxicity (that is, the toxicity class) of the contained pesticide. [1] [2] [3] The schemes follows from the Insecticides Act of 1968 [1] and the Insecticides Rules of 1971.

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  4. Pesticide formulation - Wikipedia

    en.wikipedia.org/wiki/Pesticide_formulation

    The biological activity of a pesticide, be it chemical or biological in nature, is determined by its active ingredient (AI - also called the active substance). Pesticide products very rarely consist of the pure active ingredient.

  5. Dichlorvos - Wikipedia

    en.wikipedia.org/wiki/Dichlorvos

    Dichlorvos (2,2-dichlorovinyl dimethyl phosphate, commonly abbreviated as an DDVP [1]) is an organophosphate widely used as an insecticide to control household pests, in public health, and protecting stored products from insects. The compound has been commercially available since 1961.

  6. Insect repellent - Wikipedia

    en.wikipedia.org/wiki/Insect_repellent

    Synthetic repellents tend to be more effective and/or longer lasting than "natural" repellents. [1] [2]For protection against ticks and mosquito bites, the U.S. Centers for Disease Control (CDC) recommends DEET, icaridin (picaridin, KBR 3023), oil of lemon eucalyptus (OLE), para-menthane-diol (PMD), IR3535 and 2-undecanone with the caveat that higher percentages of the active ingredient ...

  7. Pyriproxyfen - Wikipedia

    en.wikipedia.org/wiki/Pyriproxyfen

    Pyriproxyfen is a pesticide which is found to be effective against a variety of insects. [3] It was introduced to the US in 1996, to protect cotton crops against whitefly.It has also been found useful for protecting other crops. [4]

  8. Chlorfenapyr - Wikipedia

    en.wikipedia.org/wiki/Chlorfenapyr

    Chlorfenapyr was developed by American Cyanamid from the natural product dioxapyrrolomycin, which was isolated from Streptomyces fumanus. [2]The United States Environmental Protection Agency initially denied registration in 2000 for use on cotton primarily because of concerns that the insecticide was toxic to birds and because effective alternatives were available. [3]

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