Technical Report: (6616) December 05, 2016 Date Received: December 05, 2016 Page 1 of 6

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1 CONSUMER PRODUCTS SERVICES DIVISION NGBO MERRYART GLOWTECH CO., LTD Technical Report: (6616) Date Received: Page 1 of 6 TANG NGBO MERRYART GLOWTECH CO., LTD NO.8 LIXIN RD, XIAOGANG DUTOUDONG IND. PARK, BEILUN, NGBO,CHINA Sample Description: Vendor: Manufacturer: Buyer: Labeled Age Grade: Appropriate Age Grade: Client Specified Age Grade: Tested Age Grade: UPC Code: Color: BUBBLE WATER NGBO MERRYART GLOW TECH CO., LTD TRANSPARENT Sample Size: Style No(s): SKN/SKU No.: PO No.: Ref #: Country of Origin: Assortment No.: Country of Destination: 1 SET EXECUTIVE SUMMARY: The sample(s) MEETS the following requirement(s): The sample(s) was examined according to the European Pharmacopoeia 8 th Edition, Microbiological Examination of nonsterile products. The sample(s) was examined for microbial limits using the customer demand according to the European Pharmacopoeia (EP), Volume 7.0 (2011) Efficacy of Antimicrobial Preservation. The sample(s) was examined for microbial limits according to the United States Pharmacopeia USP39 NF34(2016), Microbiological Tests: <51> Antimicrobial effectiveness testing. Bureau Veritas Consumer Products Services Division (Shanghai) No. 168, Guanghua Road, Zhuanqiao Town, Minhang, Shanghai, China. Post Code: Tel: Fax: bvcps_sh_info@cn.bureauveritas.com Http: This report is governed by, and incorporates by reference, the Conditions of Testing as posted at the date of issuance of this report at and is intended for your exclusive use. Any copying or replication of this report to or for any other person or entity, or use of our name or trademark, is permitted only with our prior written permission. This report sets forth our findings solely with respect to the test samples identified herein. The results set forth in this report are not indicative or representative of the quality or characteristics of the lot from which a test sample was taken or any similar or identical product unless specifically and expressly noted. Our report includes all of the tests requested by you and the results thereof based upon the information that you provided to us. You have 60 days from date of issuance of this report to notify us of any material error or omission caused by our negligence, provided, however, that such notice shall be in writing and shall specifically address the issue you wish to raise. A failure to raise such issue within the prescribed time shall constitute your unqualified acceptance of the completeness of this report, the tests conducted and the correctness of the report contents.

2 NGBO MERRYART GLOWTECH CO., LTD Technical Report: (6616) Page 2 of 6 BVCPS (SHANGHAI) GENERAL CONTACT INFORMATION FOR THIS REPORT TELEPHONE NO.: bvcpshltoy.sh@cn.bureauveritas.com BUREAU VERITAS CONSUMER PRODUCTS SERVICE DIVISION (SHANGHAI) ROGER ZHANG DEPUTY DIRECTOR(HARDLINE AND TOY DIVISION)

3 NGBO MERRYART GLOWTECH CO., LTD Technical Report: (6616) Page 3 of 6 MICROBIOLOGICAL EXAMINATION OF NONSTERILE PRODUCTS The sample(s) was examined according to the European Pharmacopoeia 8 th Edition, Microbiological Examination of nonsterile products. Test Component (A): Bubble water EP Microbiological Examination of nonsterile products: Microbial Enumeration Tests Parameter Result Requirement Conclusion Total aerobic microbial count (TPC) <10 cfu/ml Total combined molds and yeast counts (YM) <10 cfu/ml Total viable count (TPC + YM) <10 cfu/ml <5000 cfu/ml Pass cfu/ml = colonyforming units per millilitre cfu/g = colonyforming units per gram LT = Less Than GT = Greater Than EP Microbiological examination of nonsterile products: Tests for specified microorganisms Parameter Result Requirement Conclusion Staphylococcus aureus Pass Pseudomonas aeruginosa Pass Salmonella Pass Escherichia coli Pass Biletolerant GramNegative bacteria Pass Clostridia Pass Candida albicans Pass Note: CTFA (U.S. Cosmetic, Toiletry and Fragrance Association) recommends the reporting of Total aerobic microbial count and Total combined molds and Yeast count as the Total viable count. The common acceptance criteria employed in the toy and cosmetic industry are enumerated below for reference. Category Total Viable Count Limit Recommended Acceptance limit Baby Products 100 cfu/ml(g) 500 cfu/ml(g) Products for the area of the eye All other products 1,000 cfu/ml(g) 5,000 cfu/ml(g)

4 NGBO MERRYART GLOWTECH CO., LTD Technical Report: (6616) Page 4 of 6 PERSERVATIVE EFFENCTIVENESS The sample(s) was examined for microbial limits using the customer demand according to the European Pharmacopoeia (EP), Volume 7.0 (2011) Efficacy of Antimicrobial Preservation. Test Component: Bubble water Parameter / Requirement Result (log reduction) Conclusion Day 2 Day 7 Day 14 Day 28 Bacteria (for category 2): not less than 2.0 log reduction from the initial count at 2 days, not less than 3.0 log reduction from the initial count at 7 days, and no increase from the 7 days count at 28days. Pseudomonas aeruginosa Staphylococcus aureus Yeast and Molds (for category 2): not less than 2.0 log reduction from the initial count at 14 days, and no increase from the 14 days count at 28days. Candida albicans Aspergillus brasiliensis >4.6 >4.6 >4.7 >4.3 Conclusion: The sample complies with EP requirements for antimicrobial effectiveness testing as EP

5 NGBO MERRYART GLOWTECH CO., LTD Technical Report: (6616) Page 5 of 6 PERSERVATIVE EFFENCTIVENESS The sample(s) was examined for microbial limits according to the United States Pharmacopeia USP39 NF34(2016), Microbiological Tests: <51> Antimicrobial effectiveness testing. Test Component: Bubble water Parameter / Requirement Result (log reduction) Conclusion Day 14 Day 28 Bacteria (for category 2): not less than 2.0 log reduction from the initial count at 14 days, and no increase from the 14 days count at 28days. Escherichia coli (ATCC No. 8739) Pseudomonas aeruginosa (ATCC No.9027) Staphylococcus aureus (ATCC No. 6538) >4.6 Yeast and Molds (for category 2): no increase from the initial calculated count at 14 and 28 days. Candida albicans (ATCC No ) Aspergillus niger (ATCC No ) Conclusion: The sample complies with USP requirements for antimicrobial effectiveness testing as per USP51.

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