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  2. Icaridin - Wikipedia

    en.wikipedia.org/wiki/Icaridin

    Icaridin, also known as picaridin, is an insect repellent which can be used directly on skin or clothing. [1] It has broad efficacy against various arthropods such as mosquitos, ticks, gnats, flies and fleas, and is almost colorless and odorless.

  3. Flea treatments - Wikipedia

    en.wikipedia.org/wiki/Flea_treatments

    All flea-control products are recommended to be used at least half-yearly because the lifecycle of flea can last up to a year. [5] Although these products are effective in fighting against flea and tick infestations, they have different active ingredients and, because cats cannot metabolize some of the compounds of the product, care must be ...

  4. Selamectin - Wikipedia

    en.wikipedia.org/wiki/Selamectin

    Selamectin, sold under the brand name Revolution, among others, is a topical parasiticide and anthelminthic used on dogs and cats. [2] It treats and prevents infections of heartworms, fleas, ear mites, sarcoptic mange (scabies), and certain types of ticks in dogs, and prevents heartworms, fleas, ear mites, hookworms, and roundworms in cats.

  5. Neonicotinoid - Wikipedia

    en.wikipedia.org/wiki/Neonicotinoid

    A 2013 Dutch study found that water containing allowable concentrations of imidacloprid had 50% fewer invertebrate species compared with uncontaminated water. [ 122 ] [ 123 ] A later study found the analysis was confounded with other co-occurring insecticides and did not show imidacloprid directly affected invertebrate diversity.

  6. Fipronil - Wikipedia

    en.wikipedia.org/wiki/Fipronil

    As of 2017, there does not appear to be significant resistance among fleas to fipronil. [5] Fipronil is used as the active ingredient in flea control products for pets and home roach baits as well as field pest control for corn, golf courses, and commercial turf. Its widespread use makes its specific effects the subject of considerable attention.

  7. Diazinon - Wikipedia

    en.wikipedia.org/wiki/Diazinon

    According to the German Patent bureau, the industrial synthesis of diazinon is as follows: β-isobutyrylaminocrotonic acid amine was cyclized with NaOR (R is either a hydrogen or aliphatic chain of 1 to 8 carbons) in a mixture of 0 to 100% by weight of water and an alcohol having 1 to 8 carbon atoms, above 90°C (but below the boiling point of the mixture used).

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