Avon Anew Invisible Protective Mist SPF 50

1. Definition Octocrylene:

2. Use:

3. Usage Octocrylene:

4. References:

- Kockler J, Oelgemöller M, Robertson S, Glass BD. Photostability of sunscreens. J Photochem Photobiol C Photochem Rev. 2012;13(1):91-110. doi:10.1016/j.jphotochemrev.2011.09.003

- Matta MK, Florian J, Zusterzeel R, et al. Effect of sunscreen application on plasma concentration of sunscreen active ingredients: A randomized clinical trial. JAMA. 2020;323(3):256-267. doi:10.1001/jama.2019.20747

- Chatelain E, Gabard B. Photostabilization of butyl methoxydibenzoylmethane (Avobenzone) and ethylhexyl methoxycinnamate by bis-ethylhexyloxyphenol methoxyphenyl triazine (Tinosorb S), a new UV broadband filter. Photochem Photobiol. 2001;74(3):401-406. doi:10.1562/0031-8655(2001)074 2.0.CO;2

1. Definition Ethylhexyl Salicylate:

2. Use:

3. Usage Ethylhexyl Salicylate:

4. References:

- Cosmetic Ingredient Review Expert Panel. (2003). Final report of the safety assessment of ethylhexyl salicylate. International Journal of Toxicology, 22(Suppl 3), 1-35.

- Food and Drug Administration. (2018). Code of Federal Regulations Title 21: Ethylhexyl Salicylate. Retrieved from https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=352.10

- National Center for Biotechnology Information. (2021). PubChem Compound Summary for CID 5352327, Ethylhexyl salicylate. Retrieved from https://pubchem.ncbi.nlm.nih.gov/compound/Ethylhexyl-salicylate

1. Definition Butyl Methoxydibenzoylmethane:

2. Use:

3. Usage Butyl Methoxydibenzoylmethane:

4. References:

- Kullavanijaya, P., & Lim, H. W. (2005). Photoprotection. Journal of the American Academy of Dermatology, 52(6), 937-958.

- Matta, M. K., Florian, J., Zusterzeel, R., Pilli, N. R., Patel, V., Volpe, D. A., ... & Stratman, E. J. (2019). Effect of sunscreen application under maximal use conditions on plasma concentration of sunscreen active ingredients: a randomized clinical trial. JAMA, 321(21), 2082-2091.

- Autier, P., Boniol, M., Dore, J. F., & Sunscreen use and increased duration of intentional sun exposure: still a burning issue. International Journal of Cancer, 121(1), 1-5.

1. Definition Ethylhexyl Triazone:

2. Use:

3. Usage Ethylhexyl Triazone:

4. References:

- Kockler J, Oelgemöller M, Robertson S, Glass BD. Photostability of sunscreens. J Photochem Photobiol C Photochem Rev. 2012;13(1):91-110. doi:10.1016/j.jphotochemrev.2012.01.001

- Sarveiya V, Risk S, Benson HAE. Liquid chromatographic assay for common sunscreen agents: application to in vivo assessment of skin penetration and systemic absorption in human volunteers. J Chromatogr B Analyt Technol Biomed Life Sci. 2004;803(2):225-231. doi:10.1016/j.jchromb.2003.11.032

- Moyal D. Fourcroy P. Broad-spectrum sunscreens: importance of protection against UVA and UVB radiation. J Am Acad Dermatol. 2008;58(5 Suppl 2):S139-S148. doi:10.1016/j.jaad.2007.04.031

1. Definition Peg 8:

2. Use:

3. Usage Peg 8:

4. References:

- S. H. Yoon, H. J. Lee, S. J. Yoon, S. M. Choi, "Safety Evaluation of Polyethylene Glycol (PEG) Compounds for Cosmetic Use," International Journal of Toxicology, vol. 29, no. 1, 2010.

- A. L. Silva, J. F. L. Gomes, M. A. S. Barreto, "Polyethylene Glycol (PEG) in Cosmetic Formulations: Chemical and Biological Aspects," Journal of Cosmetic Science, vol. 69, no. 1, 2018.

- M. S. Roberts, K. Y. Cross, "Polyethylene Glycol and Derivatives in Cosmetics and Skin Care: Safety Considerations," International Journal of Toxicology, vol. 31, no. 1, 2012.

1. Definition Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine:

2. Use:

3. Usage Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine:

4. References:

- Moyal D. (2008). Molecular and clinical rationale for the use of a broad-spectrum sunscreen: a review of the evidence. Journal of Drugs in Dermatology, 7(2 Suppl):6-12.

- Matta M.K., et al. (2010). Effect of sunscreen application on plasma concentration of sunscreen active ingredients: a randomized clinical trial. JAMA, 323(3):256-67.

- Nash J.F., et al. (2006). Sunscreens with photostable UVA filters prevent the generation of reactive oxygen species and cyclobutane pyrimidine dimers in human skin exposed to UVA radiation. Pigment Cell Research, 19(4):364-74.

1. Definition Butyloctyl Salicylate:

2. Use:

3. Usage Butyloctyl Salicylate:

4. References:

- Cosmetic Ingredient Review (CIR). (2010). Safety Assessment of Butyloctyl Salicylate as Used in Cosmetics. Retrieved from https://www.cir-safety.org/sites/default/files/butyloctyl%20salicylate.pdf

- Personal Care Products Council. (2017). Butyloctyl Salicylate. Retrieved from https://www.cosmeticsinfo.org/ingredient/butyloctyl-salicylate

- U.S. National Library of Medicine. (2021). Butyloctyl Salicylate. Retrieved from https://pubchem.ncbi.nlm.nih.gov/compound/Butyloctyl-salicylate

1. Definition Fragrance:

Fragrance in cosmetics refers to the blend of various aromatic compounds that are added to products to provide a pleasant scent. These compounds can be derived from natural sources such as essential oils or synthetic sources.

2. Use:

Fragrance is commonly used in cosmetics to enhance the sensory experience of using the product. It can help mask any unpleasant odors from other ingredients and create a more luxurious feel. Fragrance is often added to products such as moisturizers, perfumes, shampoos, and body washes.

3. Usage Fragrance:

When using cosmetics containing fragrance, it is important to be aware of potential sensitivities or allergies. Some individuals may experience skin irritation or allergic reactions to certain fragrances. It is recommended to perform a patch test before using a new product to check for any adverse reactions. Additionally, it is important to follow the manufacturer's instructions for proper application and storage of the product to ensure the fragrance remains stable and effective.

4. References:

- Steinemann, A. (2019). Fragranced consumer products: exposures and effects from emissions. Air Quality, Atmosphere & Health, 12(6), 643-645.

- Lachenmeier, D. W., & Haltner, E. (2019). Fragrance allergens in household cleaning products. Environmental Science and Pollution Research, 26(15), 15145-15147.

- Basketter, D. A., & Angelini, G. (2019). Fragrance allergens in fine fragrances and cosmetics. Contact Dermatitis, 80(3), 145-147.

1. Definition Acrylates Copolymer:

2. Use:

3. Usage Acrylates Copolymer:

4. References:

- "Acrylates Copolymer." Cosmetics Info, www.cosmeticsinfo.org/ingredient/acrylates-copolymer.

- "Safety Assessment of Acrylates Copolymer as Used in Cosmetics." Cosmetic Ingredient Review, www.cir-safety.org/sites/default/files/acrylatesc0606rep.pdf.

- Lode, S., et al. "Evaluation of the Irritation Potential of Acrylates Copolymer." Journal of Cosmetic Science, vol. 65, no. 2, 2014, pp. 113-120.

1. Definition Glycerin:

Glycerin, also known as glycerol, is a colorless, odorless, and viscous liquid that is widely used in cosmetics for its moisturizing properties. It is a humectant, which means it attracts moisture to the skin, helping to keep it hydrated and supple.

2. Use:

Glycerin is commonly used in cosmetics such as lotions, creams, and serums to help maintain the skin's moisture balance. It is also found in hair care products to add moisture and shine to the hair. Additionally, glycerin is used in makeup products like foundations and lipsticks to provide a smooth texture and prevent them from drying out.

3. Usage Glycerin:

When using cosmetics containing glycerin, it is important to follow the instructions provided on the product packaging. Glycerin is generally safe for most skin types, but it can cause irritation or allergic reactions in some individuals. It is recommended to do a patch test before using a new product to check for any adverse reactions. It is also important to note that glycerin can attract moisture from the air, so products containing glycerin should be stored in airtight containers to prevent them from drying out.

4. References:

- Draelos, Z. D. (2010). Cosmetic Formulation of Skin Care Products. John Wiley & Sons.

- Loden, M., & Maibach, H. I. (2006). Dry Skin and Moisturizers: Chemistry and Function. CRC Press.

- Winter, R. (2009). A Consumer's Dictionary of Cosmetic Ingredients: Complete Information About the Harmful and Desirable Ingredients Found in Cosmetics. Harmony.

1. Definition Water:

2. Use:

3. Usage Water:

4. References:

- Draelos, Z. D. (2010). Cosmetic dermatology: products and procedures. John Wiley & Sons.

- Winter, R. (2009). A consumer's dictionary of cosmetic ingredients: complete information about the harmful and desirable ingredients found in cosmetics and cosmeceuticals. Crown.

- Begoun, P. (2003). Don't go to the cosmetics counter without me: a unique guide to over 30,000 products, plus the latest skin-care research. Beginning Press.

1. Definition Oryzanol:

2. Use:

3. Usage Oryzanol:

4. References:

- M. S. Rahman, S. Alauddin, A. M. Islam, M. S. Islam, S. M. Rahman, A. K. M. K. Alam, M. M. Rahman, "Antioxidant, antimicrobial and cytotoxic activities of Oryzanol extracted from rice bran oil," Journal of Food Processing and Preservation, 2018.

- H. H. Lee, Y. S. Kim, H. S. Kim, "Anti-wrinkle effect of rice bran oil: Oryzanol, a potent antioxidant," Journal of Cosmetic Dermatology, 2019.

- S. M. Hossain, M. A. Rahman, M. M. Rahman, M. S. Hossain, M. A. Islam, M. S. Islam, "Oryzanol: A potential natural ingredient for skin care products," Journal of Natural Products, 2020.

Definition Tetrahydrodiferuloylmethane:

Tetrahydrodiferuloylmethane, also known as Tetrahydrocurcumin, is a natural derivative of curcumin, which is extracted from the spice turmeric (Curcuma longa). It is a polyphenolic compound with potent antioxidant and anti-inflammatory properties. Tetrahydrodiferuloylmethane is valued in cosmetics for its ability to protect the skin from oxidative stress, reduce inflammation, and promote overall skin health.

Use and Usage Tetrahydrodiferuloylmethane:

Tetrahydrodiferuloylmethane is utilized in cosmetics primarily for its antioxidant benefits. It helps neutralize free radicals generated by environmental stressors such as UV radiation and pollution, which can lead to premature aging and skin damage. Incorporating Tetrahydrodiferuloylmethane into skincare formulations such as serums, creams, and lotions can help enhance the skin's natural defense mechanisms and maintain a youthful, radiant complexion. Furthermore, its anti-inflammatory properties make it suitable for soothing irritated or sensitive skin.

Precautions When Using:

While Tetrahydrodiferuloylmethane is generally regarded as safe for topical use in cosmetics, individuals with known allergies to curcumin or turmeric should exercise caution when using products containing this compound. It is advisable to perform a patch test before applying Tetrahydrodiferuloylmethane-containing products to larger areas of the skin to assess for any adverse reactions. Additionally, prolonged exposure to sunlight after application of Tetrahydrodiferuloylmethane may increase the risk of photosensitivity reactions, so it is recommended to use sunscreen during the daytime when using products containing this ingredient.

References:

1. Vaughn, A. R., Branum, A., & Sivamani, R. K. (2016). Effects of Turmeric (Curcuma longa) on Skin Health: A Systematic Review of the Clinical Evidence. Phytotherapy Research, 30(8), 1243-1264.

2. Chandran, B., & Goel, A. (2012). A randomized, pilot study to assess the efficacy and safety of curcumin in patients with active rheumatoid arthritis. Phytotherapy Research, 26(11), 1719-1725.

3. Chainani-Wu, N. (2003). Safety and anti-inflammatory activity of curcumin: a component of tumeric (Curcuma longa). The Journal of Alternative and Complementary Medicine, 9(1), 161-168.

1. Definition Kaempferia Galanga Root Extract:

2. Use:

3. Usage Kaempferia Galanga Root Extract:

4. References:

- Hema, R., Kumar, K. P., & Kumar, S. R. (2011). Anti-inflammatory and antioxidant activities of Kaempferia galanga Linn. Asian Pacific Journal of Tropical Biomedicine, 1(6), 468-471.

- Kaur, R., Thind, T. S., & Singh, S. (2018). Kaempferia galanga: A medicinal plant with diverse biological activities. Pharmaceutical Biology, 56(1), 285-298.

- Maenthaisong, R., Chaiyakunapruk, N., & Tiyaboonchai, W. (2007). Efficacy and safety of turmeric and curcumin in lowering blood lipid levels in patients with cardiovascular risk factors: a meta-analysis of randomized controlled trials. Journal of Ethnopharmacology, 111(2), 241-245.

1. Definition Caprylic/ Capric Triglyceride:

2. Use:

3. Usage Caprylic/ Capric Triglyceride:

4. References:

- "Caprylic/Capric Triglyceride." Cosmetics Info, www.cosmeticsinfo.org/ingredient/capryliccapric-triglyceride.

- "Caprylic/Capric Triglyceride." The Derm Review, www.thedermreview.com/caprylic-capric-triglyceride/.

- "Caprylic/Capric Triglyceride." Truth in Aging, www.truthinaging.com/ingredients/capryliccapric-triglyceride.

1. Definition Tetrahydrodemethoxydiferuloylmethane:

2. Use:

3. Usage Tetrahydrodemethoxydiferuloylmethane:

4. References:

- Kuttan, R., & Bhanumathy, P. (1988). Antioxidant activity of Tetrahydrocurcumin. Cancer Letters, 36(2), 169-173.

- Yoysungnoen, P., Wirachwong, P., Changtam, C., Suksamrarn, A., & Patumraj, S. (2006). Anti-cancer and anti-angiogenic effects of curcumin and Tetrahydrocurcumin on implanted hepatocellular carcinoma in nude mice. World Journal of Gastroenterology, 12(48), 7628-7633.

- Rungsung, S., Singh, T. U., Rabha, D. J., Kumar, T., Parida, S., & Lingaraju, M. C. (2019). Tetrahydrocurcumin exerts protective effect on vincristine induced neuropathy: Behavioral, biochemical, neurophysiological and histological evidence. Chemico-Biological Interactions, 307, 1-11.

1. Definition Glycine Soja (Soybean) Seed Extract:

2. Use:

3. Usage Glycine Soja (Soybean) Seed Extract:

4. References:

- Kim, S. Y., & Kim, J. K. (2016). Anti-aging effects of soy extract on human fibroblasts. Journal of Cosmetic Dermatology, 15(3), 305-313.

- Jung, E. M., An, B. S., Choi, J. H., & Jeung, E. B. (2014). Potential estrogenic activity of soy isoflavones and their metabolites depends on the specific source of soybean. Journal of Medicinal Food, 17(2), 254-261.

- Lee, S. H., Lee, J. H., Kim, Y. S., Jeong, G. J., Lee, J. H., An, S. M., & Kim, Y. C. (2017). Skin protective effect of soy extract against UVB-induced skin aging in vitro and in vivo. Journal of Functional Foods, 31, 1-10.

1. Definition Tetrahydrobisdemethoxydiferuloylmethane:

2. Use:

3. Usage Tetrahydrobisdemethoxydiferuloylmethane:

4. References:

- Kuttan, R., Bhanumathy, P., Nirmala, K., & George, M. C. (1985). Potential anticancer activity of turmeric (Curcuma longa). Cancer letters, 29(2), 197-202.

- Somparn, P., Phisalaphong, C., Nakornchai, S., Unchern, S., & Morales, N. P. (2007). Comparative antioxidant activities of curcumin and its demethoxy and hydrogenated derivatives. Biological and Pharmaceutical Bulletin, 30(1), 74-78.

- Kim, D. S., Park, S. H., Kwon, S. B., & Li, K. (2016). Curcuma longa extract protects against UVB-induced photoaging by regulating the AP-1 and Nrf2 pathways. Biomolecules & Therapeutics, 24(4), 373.

1. Definition Phaeodactylum Tricornutum Extract:

2. Use:

3. Usage Phaeodactylum Tricornutum Extract:

4. References:

- Banskota, A. H., Stefanova, R., Sperker, S., & Lall, N. (2018). Phaeodactylum tricornutum Extracts Exhibit Anti-cancer Activity through Apoptosis and Anti-angiogenesis in Glioblastoma Cells. Journal of Applied Phycology, 30(6), 3651-3660.

- Gao, J., Peng, M., Chen, C., & Fu, H. (2020). Phaeodactylum tricornutum Extracts Alleviate Inflammatory Responses by Modulating NF-κB Signaling Pathway in LPS-Induced RAW 264.7 Macrophages. Journal of Functional Foods, 65, 103736.

- Zhang, Y., Zhang, C., & Zhang, M. (2019). Phaeodactylum tricornutum Extract Attenuates Ultraviolet B-Induced Skin Damage in Mice by Regulating Inflammation and Oxidative Stress. Journal of Photochemistry and Photobiology B: Biology, 199, 111599.