Record and test items of domestic special purpose cosmetics

Examine project of application for sanitary administrative licensing of domestic specifc function cosmetics

category          Inspection items                                                                                                        Number of samples                 Inspection cycle

Perm      mercury arsenic lead Mercaptoacetic acid pH Eye irritation Acute skin irritation and skin allergy.         14individual                    60day

Deodorization      mercury arsenic lead formaldehyde Safety evaluation of repeated skin irritation skin allergy and human trial test.    16individual                   80day

Depilation      mercury arsenic lead Mercaptoacetic acid pH Safety evaluation of skin allergy and human trial test.            16individual                   80day

Freckle removing class    microorganism mercury arsenic lead Argon quinone phenol pH Multiple skin irritation(Cleansing/Shampoo does not do thisterm,Another acute skin irritation Eye irritation) Skin allergy Skin phototoxicity and human patch. 19individual   80day

Sunscreen       microorganism mercury arsenic lead Ultraviolet absorber SPF value(Official biographySPFValue products), PAvalue(Should not measure the human bodySPFTime  19 80day/140day

Hair dyeing      mercury arsenic lead Dye intermediate Eye irritation,Skin allergy Salmonella typhimurium reverse mutation(Ame's)Chromosome aberrations of mammalian cells in vitro.  17individual  80day

Beauty Milk    microorganism mercury,arsenic lead,sex hormone Multiple skin irritation Skin allergy Ame's in vitro20individual+60people1Months150day( Including chromosome aberration of human body-building mammalian cells and safety evaluation of human trial test.  

Hair raising class     microorganism(Alcohol degree≥75%do not do) mercury arsenic lead Cantharides Nitrogen mustard sex hormone Eye irritation many22individual+70people2Months180day(includeImprove skin irritation Skin allergy Skin phototoxicity Ame' 8 Amount of mammalian cell chromosomes in vitro  Distortion during human trial and safety evaluation of human trial test.)

Specific contents of domestic special purpose cosmetics filing

①Complete the collection of declaration and regulatory documents,And read,Clear declaration requirements;②Declared product formula The production process has been determined,And completed the relevant key indicators of risk(Such as residual excitability SPFQiao et al)of Preamble test ;③Reported to local competent department[ ]Make clear the declaration procedures and requirements.

  ①The firstICompletion of preparation of stage application materials,Binding according to the number and order of copies submitted Signature and seal,Prepare for submission;②Formulate the implementation plan for the rectification of the hygienic conditions at the production site,Prepare for rectification Welcome the audit of on-site hygiene and production capacity conditions.

  ①Complete section1Submission of stage application materials,obtain Notification of acceptance ;②Complete the rectification of sanitary conditions at the production site,Waiting for on-site review;③The inspection organization is determined,The inspection requirements are clear.

  ①adopt On site audit of production hygiene conditions";②Samples for inspection are ready;③The first1The materials reported in the stage have passed the review of the provincial food and drug administration,Obtain its signature and seal The first1Stage application materials .

  ①Complete section2Stage application materials,And meet the submission requirements;②Materials and samples shall be submitted to the inspection agency,The product enters the inspection stage.

  ①Complete section3Stage application materials;②Online application unit user name and password ,Complete online declaration;③Obtain the qualified certificate issued by the inspection organization Inspection report And related information.

  ①Complete the second step as required3Stage cascade report materials;②Submit it to the acceptance center of the State Food and Drug Administration in Beijing,And obtain Notification of acceptance .

  Pass the review,Then obtain Approval document ; Last pass,Then press Notice of correction do Correction materials And submit;It is necessary to apply for reconsideration, Apply for reconsideration .

  Go to Beijing to get the approval documents for declaration,Namely Approval number .

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