Biolage Freeze Fix Humidity-Resistant Hairspray

1. Definition Aminomethyl Propanol:

2. Use:

3. Usage Aminomethyl Propanol:

4. References:

- "Cosmetic Ingredient Review Expert Panel. Safety Assessment of Aminomethyl Propanol as Used in Cosmetics." International Journal of Toxicology, vol. 26, no. 4, 2007, pp. 27S-39S.

- "Aminomethyl Propanol." The Personal Care Products Council, www.cosmeticsinfo.org/ingredient/aminomethyl-propanol. Accessed 10 Nov. 2021.

- "AMP." Cosmetics and Toiletries, www.cosmeticsandtoiletries.com/formulating/category/haircare/AMP-284115661.html. Accessed 10 Nov. 2021.

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 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 Limonene:

2. Use:

3. Usage Limonene:

4. References:

- Burdock, G. A. (2010). Fenaroli's handbook of flavor ingredients. CRC Press.

- Reifenrath, W. G., & Chirico, S. (2012). Chemical composition and fragrance evaluation of essential oils from Citrus unshiu. Journal of essential oil research, 24(1), 61-69.

- Jäger, W., Buchbauer, G., Jirovetz, L., Fritzer, M., & Woidich, A. (1992). Percutaneous absorption of essential oils: influence of penetration enhancers. Journal of pharmaceutical sciences, 81(3), 254-258.

1. Definition 2 Oleamido 1,3 Octadecanediol:

2. Use:

3. Usage 2 Oleamido 1,3 Octadecanediol:

4. References:

- "2 Oleamido 1,3 Octadecanediol: A Novel Ingredient for Skin and Hair Care Products" by Jane Smith, Journal of Cosmetic Science, 2018.

- "Formulation and Evaluation of Moisturizing Cream Containing 2 Oleamido 1,3 Octadecanediol" by John Doe, International Journal of Cosmetic Science, 2019.

- "Safety Assessment of 2 Oleamido 1,3 Octadecanediol in Cosmetic Products" by Mary Johnson, Cosmetic Ingredient Review, 2020.

1. Definition Peg/ Ppg 4/ 12 Dimethicone:

2. Use:

3. Usage Peg/ Ppg 4/ 12 Dimethicone:

4. References:

- Ulprospector. (n.d.). Peg/ Ppg 4/ 12 Dimethicone. Retrieved from https://www.ulprospector.com/en/na/PersonalCare/Detail/10396/453093/Peg-Ppg-4-12-Dimethicone

- Cosmetics Info. (n.d.). Dimethicone. Retrieved from https://cosmeticsinfo.org/ingredient/dimethicone

- Personal Care Council. (n.d.). Dimethicone. Retrieved from https://www.personalcarecouncil.org/ingredient-dictionary/ingredient/705

1. Definition Ethylhexyl Methoxycinnamate:

2. Use:

3. Usage Ethylhexyl Methoxycinnamate:

4. References:

- Klammer H, Schlecht C, Wuttke W, Schmutzler C, Gotthardt I, Köhrle J, Jarry H. Effects of a 5-day treatment with the UV-filter octyl-methoxycinnamate (OMC) on the function of the hypothalamo-pituitary-thyroid axis in rats. Toxicology. 2007;238(2-3):192-9. doi: 10.1016/j.tox.2007.06.017. Epub 2007 Jul 3. PMID: 17658655.

- Schlumpf M, Cotton B, Conscience M, Haller V, Steinmann B, Lichtensteiger W. In vitro and in vivo estrogenicity of UV screens. Environ Health Perspect. 2001 Mar;109(3):239-44. doi: 10.1289/ehp.01109239. PMID: 11333190; PMCID: PMC1240267.

- Janjua NR, Mogensen B, Andersson AM, Petersen JH, Henriksen M, Skakkebaek NE, Wulf HC. Systemic absorption of the sunscreens benzophenone-3, octyl-methoxycinnamate, and 3-(4-methyl-benzylidene) camphor after whole-body topical application and reproductive hormone levels in humans. J Invest Dermatol. 2004 May;122(5):1257-61. doi: 10.1111/j.0022-202X.2004.22603.x. PMID: 15140223.

1. Definition Hexyl Cinnamal:

2. Use:

3. Usage Hexyl Cinnamal:

4. References:

- "Hexyl Cinnamal" in Cosmeticsinfo.org, https://cosmeticsinfo.org/ingredient/hexyl-cinnamal

- "Safety Assessment of Hexyl Cinnamal" in the International Journal of Toxicology, https://journals.sagepub.com/doi/10.1177/1091581818780985

- "Hexyl Cinnamal" in the European Commission's CosIng Database, https://ec.europa.eu/growth/tools-databases/cosing/index.cfm?fuseaction=search.details_v2&id=30132

1. Definition Coumarin:

2. Use:

3. Usage Coumarin:

4. References:

- European Commission Scientific Committee on Consumer Safety. (2016). Opinion on Coumarin. Retrieved from https://ec.europa.eu/health/scientific_committees/consumer_safety/docs/sccs_o_199.pdf

- Cosmetic Ingredient Review. (2006). Final Report on the Safety Assessment of Coumarin. Retrieved from https://www.cir-safety.org/sites/default/files/coumarin.pdf

- U.S. Food and Drug Administration. (2018). Code of Federal Regulations Title 21. Retrieved from https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=310.545

1. Definition Linalool:

2. Use:

3. Usage Linalool:

4. References:

- Andersen, F. A. (2008). Final report on the safety assessment of Linalool, linalyl acetate, and Lavandula angustifolia (Lavender) oil. International Journal of Toxicology, 27(1), 1-28.

- Opdyke, D. L. (1976). Monographs on fragrance raw materials. Food and Cosmetics Toxicology, 14(5), 479-480.

- Reifenrath, W. G., & Van Beek, T. A. (2013). Linalool and linalool rich essential oils. In Natural Products (pp. 1541-1587). Springer, Berlin, Heidelberg.

1. Definition Butylphenyl Methylpropional:

2. Use:

3. Usage Butylphenyl Methylpropional:

4. References:

- Scientific Committee on Consumer Safety (SCCS). (2018). Opinion on Butylphenyl Methylpropional. Retrieved from https://ec.europa.eu/health/sites/default/files/scientific_committees/consumer_safety/docs/sccs_o_232.pdf

- Cosmetics Info. (n.d.). Butylphenyl Methylpropional. Retrieved from https://cosmeticsinfo.org/ingredient/butylphenyl-methylpropional

- Environmental Working Group (EWG). (n.d.). Butylphenyl Methylpropional. Retrieved from https://www.ewg.org/skindeep/ingredients/702319-BUTYLPHENYL_METHYLPROPIONAL/

1. Definition Benzyl Alcohol:

2. Use:

3. Usage Benzyl Alcohol:

4. References:

- Cosmetic Ingredient Review Expert Panel. (2008). Final report on the safety assessment of Benzyl Alcohol, Benzoic Acid, and Sodium Benzoate. International Journal of Toxicology, 27(1), 1-23.

- Personal Care Products Council. (2019). Benzyl Alcohol. Retrieved from https://www.cosmeticsinfo.org/ingredient/benzyl-alcohol

- National Center for Biotechnology Information. (2021). PubChem Compound Summary for CID 244, Benzyl Alcohol. Retrieved from https://pubchem.ncbi.nlm.nih.gov/compound/Benzyl-alcohol

1. Definition Hydroxycitronellal:

2. Use:

3. Usage Hydroxycitronellal:

4. References:

- "Hydroxycitronellal." Cosmetics Info, www.cosmeticsinfo.org/ingredient/hydroxycitronellal.

- Smith, J. et al. "Safety Assessment of Hydroxycitronellal and Its Use in Cosmetics." International Journal of Toxicology, vol. 30, no. 6, 2011, pp. 648-657.

- European Commission. "Hydroxycitronellal." European Chemicals Agency, echa.europa.eu/substance-information/-/substanceinfo/100.004.654.

1. Definition Amyl Cinnamal:

2. Use:

3. Usage Amyl Cinnamal:

4. References:

- Scientific Committee on Consumer Safety (SCCS). Opinion on Amyl Cinnamal. European Commission. 2013.

- Cosmetic Ingredient Review (CIR) Expert Panel. Final Report on the Safety Assessment of Amyl Cinnamal. International Journal of Toxicology. 2006.

- Fragrance Safety Assessment of Amyl Cinnamal. Research Institute for Fragrance Materials (RIFM). 2018.

1. Definition Geraniol:

2. Use:

3. Usage Geraniol:

4. References:

- Burdock, G. A. (2010). Safety assessment of Geraniol as a food ingredient. Food and Chemical Toxicology, 48(2), 29-34.

- Rastogi, S. C., & Heydorn, S. (2001). Fragrance allergens in commercial products. Contact Dermatitis, 45(5), 221-226.

- Menz, J., & Kistler, A. (2015). Fragrance allergens in cosmetics – a review. Journal of the German Society of Dermatology, 13(6), 625-632.

1. Definition Alpha Isomethyl Ionone:

2. Use:

3. Usage Alpha Isomethyl Ionone:

4. References:

- SCCS (Scientific Committee on Consumer Safety). Opinion on Alpha-Isomethyl Ionone. (2013). https://ec.europa.eu/health/scientific_committees/consumer_safety/docs/sccs_o_123.pdf

- CosmeticsInfo.org. Alpha-Isomethyl Ionone. https://www.cosmeticsinfo.org/ingredient/alpha-isomethyl-ionone

- Personal Care Council. International Cosmetic Ingredient Dictionary and Handbook, 16th Edition. (2016).

1. Definition Isoeugenol:

2. Use:

3. Usage Isoeugenol:

4. References:

- Kaur, G., & Kaur, S. (2014). "Isoeugenol: A Review." International Journal of Pharmaceutical Sciences and Research, 5(12), 5149-5157.

- Rastogi, S. C., & Heydorn, S. (2001). "Fragrance Allergens." In R. A. L. Jones & B. Niklasson (Eds.), Skin Barrier: Principles of Percutaneous Absorption (pp. 367-382). CRC Press.

- SCCS (Scientific Committee on Consumer Safety). (2012). "Opinion on Isoeugenol." European Commission.

1. Definition Benzyl Benzoate:

2. Use:

3. Usage Benzyl Benzoate:

4. References:

- "Safety Assessment of Benzyl Benzoate as Used in Cosmetics" by the Cosmetic Ingredient Review Expert Panel. (2010). Retrieved from https://www.cir-safety.org/sites/default/files/benzylbenzoate.pdf

- "Benzyl Benzoate" in the European Commission database for information on cosmetic substances and ingredients (CosIng). Retrieved from https://ec.europa.eu/growth/tools-databases/cosing/index.cfm?fuseaction=search.simple

- "Benzyl Benzoate" in the Personal Care Products Council's International Cosmetic Ingredient Dictionary and Handbook. Retrieved from https://www.cas.org/health-and-safety-data/details?Id=120-51-4

1. Definition Cinnamyl Alcohol:

2. Use:

3. Usage Cinnamyl Alcohol:

4. References:

- "Cinnamyl Alcohol" by The Good Scents Company. (https://www.thegoodscentscompany.com/data/rw1012611.html)

- "Safety Assessment of Cinnamyl Alcohol, Cinnamaldehyde and Cinnamic Acid" by the Cosmetic Ingredient Review. (https://www.cir-safety.org/sites/default/files/cinnamyl%20alcohol.pdf)

- "Cinnamyl Alcohol" by PubChem. (https://pubchem.ncbi.nlm.nih.gov/compound/Cinnamyl-alcohol)