《麥高臣 MicrocynAH》洗耳水 Ear Rinse 4oz｜無毒、無刺激，預防耳朵感染｜效期至2022年11月
NT$ 588
唯一你可以信賴的真正寵物神仙水！在過去十年Microcyn專利技術已經成功幫助上千萬的患者，包括人類及動物。由三十次的臨床試驗和數千獸醫診所證明安全有效。Microcyn專有的HOCI動物保健產品高度穩定，有效且無毒性。
■ 使用Microcyn專利技術，不傷害健康細胞，快速安全有效。
■ 潔淨、預防耳垢問題。
■ 每天使用耳朵更乾淨。
■ 不含酒精，類固醇，抗生素或茶樹精油。
■ 無毒，無刺激性。
■ 適用於所有年齡階段的動物及人類皮膚。
■ 經美國數千間獸醫院診所推薦使用。
【產品規格】
■ 主要成份：次氯酸 0.0085。
■ 非活性成份：水、硫酸鈉、磷酸鈉、氯化鈉。
■ 容量：4oz。
■ 產地：墨西哥。
■ 適用對象：犬/貓。
尚有庫存
《麥高臣 MicrocynAH》洗耳水 Ear Rinse
麥高臣以專利技術研製自身免疫系統中的次氯酸，真正天然的配方，不傷害健康細胞，對身體和環境都無毒及無害，且不會造成刺激。天然安全，動物舔食無需顧慮，對身體和環境無害。不含酒精、抗生素、類固醇。
（並非所有以次氯酸為主的動物護理產品都一樣）
產品特色
注意事項
請勿把本產品轉至其他容器保存。
請勿把本產品放置冰箱內。
請存放陰涼乾燥的地方，避免陽光直射。
【產品規格】
■ 主要成份：次氯酸 0.0085。
■ 非活性成份：水、硫酸鈉、磷酸鈉、氯化鈉。
■ 容量：4oz。
■ 產地：墨西哥。
■ 適用對象：犬/貓。
使用方式
-
如果有必要，請定期清理耳朵裡面多餘的毛髮。
-
滴適量神仙洗耳水至耳朵內，輕輕按摩耳根。
-
寵物搖頭後便可除去過量的耳液，再用棉花將多餘的神仙洗耳水擦淨，無須清洗。
-
本品不適用於內耳感染。
檢驗相關文獻
EN 1276 QUANTITATIVE SUSPENSION TEST OF BACTERICIDAL ACTIVITY OF CHEMICAL DISINFECTANTS
Summary of Test
The EN method below are designed to evaluate the bactericidal, fungicidal, yeasticidal, basic sporicidal or mycobactericidal activity of a product used under various conditions. Many methods are suspension based and are used to support general antimicrobial claims while other test methods are carrier-based and are used to support antimicrobial activity of products on surfaces or devices. In either case, the same general principles apply. The test organism is exposed to sample of the product in a manner which simulates the desired claim. Following exposure, the test system is neutralized and quantitatively assayed for survivors. The resulting plates are incubated, enumerated, and a reduction in viability or microbiocidal effect is determined as compared to a population control.
|
Test Organisms |
Staphylococcus aureus, Pseudomonas aeruginosa, Enterococcus hirae, Escherichia coli |
|
Purpose of Test |
Suspension-based study formally used to evaluate bactericidal activity. |
|
Typical Performance Criteria (Requirements may vary by claim) |
5 log reduction in ≤5 minutes |
EN 1650 QUANTITATIVE SUSPENSION TEST FOR THE EVALUATION OF FUNGICIDAL ACTIVITY OF CHEMICAL DISINFECTANTS
Summary of Test
The EN method below are designed to evaluate the bactericidal, fungicidal, yeasticidal, basic sporicidal or mycobactericidal activity of a product used under various conditions. Many methods are suspension based and are used to support general antimicrobial claims while other test methods are carrier-based and are used to support antimicrobial activity of products on surfaces or devices. In either case, the same general principles apply. The test organism is exposed to sample of the product in a manner which simulates the desired claim. Following exposure, the test system is neutralized and quantitatively assayed for survivors. The resulting plates are incubated, enumerated, and a reduction in viability or microbiocidal effect is determined as compared to a population control.
|
Test Organisms |
Candida albicans, Aspergillus brasiliensis |
|
Purpose of Test |
Suspension-based study formally used to evaluate fungicidal activity. |
|
Typical Performance Criteria |
4 log reduction in ≤15 minutes |
EN 14476 QUANTITATIVE SUSPENSION TEST FOR THE EVALUATION OF VIRUCIDAL ACTIVITY OF CHEMICAL DISINFECTANTS AND ANTISEPTICS IN HUMAN MEDICINE
Purpose of Test
The purpose of this test is to determine the minimum virucidal activity of a chemical disinfectant in contact with medical instruments, surfaces or hands, according to EN test methods developed by the CEN (European Committee for Standardization) to support registrations within Europe. The method described is intended to determine the activity of chemical disinfectants that form a homogeneous, physically stable preparation in hard water – or in the case of ready-to-use products – with deionized water, and in the conditions in which they are used.
Summary of Test
A suspension of virus is added to a solution of interfering substances; the interfering substance used is dependent on the product claim. The prepared test product is added to the suspension of virus in interfering substance and is maintained at the requested temperature for the requested exposure time(s). At the end of the exposure time, aliquots are taken and the virucidal activity against the test virus is immediately neutralized or suppressed by dilution in ice-cold test medium. Serial dilutions are performed and the dilutions are then assayed for viral infectivity by an assay method specific for the testing virus. Appropriate controls are performed in parallel with the assay. Reduction of virus infectivity is calculated from differences of log virus titers before and after treatment with the product.
|
Test Organisms |
Adenovirus, Poliovirus Bovine, Parvovirus, and additional pathogens |
|
Purpose of Test |
Suspension-based study used as a presumptive test to evaluate virucidal activity. |
|
Typical Performance Criteria |
4 log reduction |
EN 13704 QUANTITATIVE SUSPENSION TEST FOR THE EVALUATION OF SPORICIDAL ACTIVITY OF CHEMICAL DESINFECTANTS USED IN FOOD, INDUSTRIAL, DOMESTIC AND INSTITUTIONAL AREAS
Purpose of test
Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants used in food, industrial, domestic and institutional areas. Not suited in situations where disinfection is medically indicated or when products are used on living tissues with the exception for hand hygiene in the above instances.
Products that can be tested
Chemical disinfectant products that form homogenous, physically stable preparations in hard water for use in the above instances.
Description of Test
· A test suspension of Bacillus subtilis spores in a solution of interfering substance, simulating clean conditions, is added to a prepared sample of the product under test diluted in hard water.
· The mixture is maintained at 20°C ± 1°C for 60 minutes ± 10 seconds.
· At the end of the contact time, a portion is taken and the sporicidal action in this portion is immediatedly neutralized or suppressed by a validated method.
The number of surviving bacterial spores in each sample are determined. The reduction in viable counts is calculated.
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