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Transcription:

Product Information Dossier (PI) Product PD210 Date May 2015 Revision 5

Contents PRODUCT INFORMATION Trade Name & Code 3 Manufacturer 3 INCI name 3 Composition 4 Additional information on ingredients 4 Specifications 5 Storage 6 Shelf life 6 Impurities 6 Regulatory status 6 REACH 7 Statements 7 MANUFACTURING FLOWCHART 9 SAFETY 10 ADDITIONAL INFORMATION 11 2

Product Information Trade Name & Code TRADE NAME CODE PD210 Manufacturer LIPOTEC S.A.U. C/ ISAAC PERAL 17, POL. IND. CAMÍ RAL 08850 GAVÀ (BARCELONA) SPAIN INCI name BUTYLENE GLYCOL, WATER (AQUA), ACETYL HEAPEPTIDE-38. 3

Composition INGREDIENT % CAS EINECS Butylene Glycol Up to 100% 107-88-0 203-529-7 Water (Aqua) 42.4575 57.4425% 7732-18-5 231-791-2 Acetyl Hexapeptide-38 0.0425 0.0575% 1400634-44-7 - Additional information on ingredients INGREDIENT Butylene Glycol Water (Aqua) Acetyl Hexapeptide-38 FUNCTION Solvent Solvent Active ingredient vegetal origin: (none) biosynthetic origin: (none) animal origin: (none) synthetic origin: Butylene Glycol, Acetyl Hexapeptide-38; mineral origin: Water (Aqua). 4

Specifications Analytical Data TEST SPECIFICATION METHOD Physical appearance Transparent solution CC-10-01-B6 Colour Colourless CC-10-01-B6 Specific gravity 0.97 1.07 CC-10-01-B3 ph N.A. Viscosity (cps) N.A. Particle size (mm) N.A. Refractive index 1.372 1.412 CC-10-01-B4 Dry residue (%) N.A. Identification (HPLC) Similar retention CC-10-01-B19 time as in-house ref. standard Microbiological Data TEST SPECIFICATION METHOD TOTAL AEROBIC MICROBIAL COUNT < 100 cfu/g MI-10-01-D09 TOTAL YEAST AND MOULD COUNT < 10 cfu/g MI-10-01-D09 SPECIFIC MICROORGANISMS: Escherichia coli ABSENCE/0.5 g MI-10-01-D09 Pseudomonas aeruginosa ABSENCE/g MI-10-01-D09 Staphylococcus aureus ABSENCE/g MI-10-01-D09 Candida albicans ABSENCE/g MI-10-01-D09 Remarks Contains 0.05% ADIFYLINE peptide. 5

Storage should be stored in a clean, cool and dark place. Shelf life If stored as recommended, shelf life is 24 months. Impurities ANALYSIS AVAILABLE EPECTED RESULT/COMMENTS Heavy metals - Diethylene Glycol NO NO Not expected based on product knowledge Other impurities - Regulatory status Information on the regulatory status of is given to the best of our knowledge in the chart below: REGION STATUS European Union In accordance with Regulation 1223/2009 on cosmetic products U.S.A. No ingredient restrictions known on cosmetic regulations No ingredient listed in California s Proposition 65 Japan No ingredient restrictions known on cosmetic regulations Brazil In accordance with Resolution RDC No.3 of January 18, 2012 Australia All ingredients listed in AICS 1 schedule Exception: Acetyl Hexapeptide-38* No ingredients listed in SUSMP 2 China All ingredients listed in IECIC schedule Exception: Acetyl Hexapeptide-38 Canada No ingredient listed in HOTLIST schedule 1 AICS: Australian Inventory of Chemical Substances 2 SUSMP: Standard for the Uniform Scheduling of medicines and Poisons *The obligation to notify to NICNAS applies only to import volumes over 10 kg of substance/year 6

REACH INGREDIENT STATUS COMMENTS Butylene Glycol Registered - Water (Aqua) Exempt (Annex IV/V) - Acetyl Hexapeptide-38 Exempt (< 1 Tonne/year) - Statements STATEMENT YES/NO COMMENTS Does the product contain any genetically modified ingredient? Does the product contain as an ingredient any of the 26 substances listed in Annex III of Cosmetics Regulation (EC) 1223/2009 and identified by the SCCNFP as likely to cause allergenic reactions? Has the product undergone animal tests sponsored by Lipotec S.A.U.? Is the product expected to contain any pesticide? Does the product contain as an ingredient any substance classified as CMR (Carcinogenicity, Germ Cell Mutagenicity and Reproductive Toxicity) from classes 1A, 1B or 2 in accordance with CLP Regulation 1272/2008 and its subsequent amendments? Does the product contain, as an ingredient, any of the following glycol ethers? EDGME (CAS nº 110-71-4) DEDGME (CAS nº 111-96-6) TEDGME (CAS nº 112-49-2) EGBE (CAS nº 111-76-2) DEGBE (CAS nº 112-34-5) DEGEE (CAS nº 111-90-0) 7

Does the product contain, as an ingredient, any phthalate? Is the product expected to contain any nanomaterial meaning an insoluble or biopersistant and intentionally manufactured material with one or more external dimensions, or an internal structure, on the scale from 1 to 100 nm, as defined in Regulation (EC) No 1223/2009 on cosmetic products? Is the product expected to contain gluten? Does the product contain any ingredient that, according to the information provided by our suppliers, falls under the definition of Volatile Organic Compound (VOC) as described in Directive 2004/42/CE? Is there risk of contamination with Bovine Spongiform Encephalopathy (BSE) through the use of this product? * - Is the product expected to contain any dioxin? Does the product contain ethanol as an ingredient? Is the product suitable for vegetarians? YES - Is the product suitable for vegans? YES - * According to the information provided by supplier, the following ingredients fall under the definition of Volatile Organic Compound (VOC) as described in Directive 2004/42/CE: Butylene Glycol. Please, note that this ingredient is not listed in Annex I of the Swiss Ordinance 814.018. 8

Manufacturing flowchart The product is manufactured according to the manufacturing standard protocol: ACTIVE INGREDIENT SOLVENT SOLVENT Check product specifications PD210 9

Safety The toxicological profile of ADIFYLINE peptide for cosmetic purposes was assessed in vitro and in vivo. IN VITRO TESTS Cytotoxicity test on human epidermal keratinocytes ADIFYLINE peptide showed no significant signs of cytotoxicity at the concentrations assayed. Cytotoxicity test on 3T3 fibroblasts ADIFYLINE peptide proved to have cytotoxic effects only at the highest tested concentration (7 mg/ml). Ocular irritation (HET-CAM test) ADIFYLINE peptide showed no ocular irritation at the tested concentrations. Phototoxicity (NRU test) ADIFYLINE peptide showed no signs of phototoxicity at the concentrations assayed. Bacterial reverse mutation test (Ames test) ADIFYLINE peptide produced no mutagenic activity in any of the bacterial strains tested. IN VIVO TESTS Skin sensitisation (HRIPT test) A HRIPT (Human Repeated Insult Patch Test) was performed on 100 volunteers aged 18 to 70. ADIFYLINE peptide 0.1% induced neither irritation nor any allergic reaction. A full toxicological report and a summary of all the safety tests performed are available on request. 10

Additional Information DOCUMENTATION AVAILABLE NOT AVAILABLE Technical Report Brochure Efficacy Reports Stability Report Qualitative Analysis Quantitative Analysis Complete Tox Toxicity Summary Safety Dossier Safety Data Sheet The trademarks referenced in this presentation are owned by The Lubrizol Corporation. Note: Graphs and photographs of efficacy tests are available for customer use provided that the final product contains the same concentration of active as the formulations in our tests. Customers must request written permission for use of the graphic material and/or ingredient tradenames to Lubrizol. Customers are responsible for compliance with local and international advertising regulations. The specific situation of the trademark in each country may vary and we recommend that you contact us for updated information. Disclaimer: The information including the claims and supporting data provided in this publication are provided for informational purposes only, upon the express condition that the User make its own assessment of the appropriate use of such information. While the information contained herein is believed to be reliable, there are no representations, guarantees, or warranties of any kind made as to its accuracy, suitability for particular applications, how the product(s) will perform in combination with other substance or in the User s process or the results obtained. All expressed and implied warranties are disclaimed. Lubrizol and its affiliates MAKE NO WARRANTIES, EPRESS OR IMPLIED, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE. The User is solely responsible for ensuring that products marketed to consumers comply with all relevant laws and regulations and assumes all risk and liability of any use or handling of any materials. User agrees to indemnify and hold harmless Lubrizol and its affiliates for any and all actions arising from User s use of any information including claims in this publication, including, but not limited to, use in advertising and finished product label claims, and not present this publication as evidence of finished product claim substantiation to any regulatory authority. It is the User s sole responsibility to determine if there are any issues relating to patent infringement relating to the supplied information. Nothing contained herein is to be considered as permission, recommendation, nor as an inducement to practice any patented invention without permission of the patent owner. 2013-2015 The Lubrizol Corporation. All Rights Reserved. 11