Overview
Octocrylene is a compound often used as an additive in sun screen, and is thought to have skin moisturizing effects because of its emollient properties. What makes this chemical such a popular additive to sun block, is its ability to neutralize UV radiation dissipated by sunlight, and to minimize skin damage from prolonged sun exposure. Octocrylene is also often combined with avobenzone, another common sunscreen ingredient often appearing on ingredient labels. Because of its effectiveness, the chemical has been approved across the globe for use in cosmetics and skin care products, but the concentrations of this ingredient are usually limited to no more than 10 or 12 percent. However, the use of this chemical doesn’t just stop with sunscreen for face and arms, but can extend to a variety of other products, like hair spray, tannin oil, BB cream, conditioner, and CC cream, among others. Octocrylene may cause contact and photocontact allergy.
Indication
In the US, Octocrylene has been evaluated by the FDA and is considered safe for use up to 10% in the formula. Similarly, the EU allows its use up to 10% in a formula while Health Canada allows a maximum use level of 12%.
Associated Conditions
- Sunburn
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
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No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Kenvue Brands LLC | 69968-0601 | TOPICAL | 100 mg in 1 g | 7/1/2025 | |
Kenvue Brands LLC | 69968-0828 | TOPICAL | 100 mg in 1 mL | 7/1/2025 | |
The Procter & Gamble Manufacturing Company | 84126-153 | TOPICAL | 6 g in 100 g | 6/9/2025 | |
BENOW BEAUTY INC | 85550-001 | TOPICAL | 5 g in 100 mL | 4/14/2025 | |
Valu Merchandisers | 63941-929 | TOPICAL | 80 mg in 1 g | 7/7/2025 | |
OL PHARMA TECH LLC. (Drs. Pharmacy) | 80489-235 | TOPICAL | 10 g in 100 g | 3/24/2025 | |
BEL STAR SA | 14141-405 | TOPICAL | 100 mg in 1 mL | 4/28/2025 | |
Kenvue Brands LLC | 69968-0816 | TOPICAL | 100 mg in 1 g | 7/1/2025 | |
Kenvue Brands LLC | 69968-0702 | TOPICAL | 100 mg in 1 mL | 7/1/2025 | |
Murad, LLC | 70381-131 | TOPICAL | 7.5 g in 100 mL | 3/26/2025 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
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No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
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No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
NUTRIMETICS SUN DAYS SUNSCREEN LOTION SPF 50+ | 219482 | Medicine | A | 1/22/2014 | |
Bondi Sands SPF 50+ Coconut Sunscreen Lotion | 319232 | Medicine | A | 6/24/2019 | |
Ecosol SPF50+ Lip Balm | 288577 | Medicine | A | 5/4/2017 | |
LA ROCHE-POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS DRY TOUCH GEL CREME TINTED SPF50+ | 297587 | Medicine | A | 12/15/2017 | |
Carroten Omega Care Suncare Oil SPF30 | 304820 | Medicine | A | 6/20/2018 | |
Cancer_Council Ultra Sunscreen Spray SPF50+ | 274939 | Medicine | A | 5/3/2016 | |
BONDI SANDS SPF50+ COCONUT BEACH SUNSCREEN LOTION | 289337 | Medicine | A | 5/25/2017 | |
BHC Skin Care Facial Sunscreen SPF 50+ | 271593 | Medicine | A | 2/29/2016 | |
Sea & Ski SPF50+ Sports and Outdoors | 236715 | Medicine | A | 4/28/2015 | |
Protection Plus Daily SPF50+ Broad Spectrum Cream | 226086 | Medicine | A | 7/22/2014 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
BRIGHT BOOST MOISTURIZER SPF 30 | johnson & johnson inc | 02488116 | Lotion - Topical | 6 % / W/W | 1/6/2020 |
BULL FROG WATER ARMOR SPORT QUICK SPRAY SUNSCREEN BROAD SPECTRUM SPF 50 | sun & skin care research inc | 02411113 | Spray - Topical | 2 % / W/W | N/A |
BOTANICAL EFFECTS HYDRATE & PROTECT BROAD SPECTRUM SUNSCREEN SPF 30 | mary kay cosmetics ltd | 02401282 | Lotion - Topical | 2.0 % / W/W | N/A |
BROAD SPECTRUM SPF 30 SPORT SUNSCREEN CONTINUOUS SPRAY | prime enterprises, llc | 02397978 | Spray, Bag-On-Valve - Topical | 2.75 % / W/W | 8/19/2013 |
OLAY COMPLETE 30 UVA/UVB 365 DAILY MOISTURIZING LOTION WITH SPF BROAD SPECTRUM SPF 30 SENSITIVE | procter & gamble inc | 02461188 | Lotion - Topical | 2.5 % / W/W | 1/1/2018 |
ROSALIAC UV LEGERE | laboratoires la roche-posay canada | 02330792 | Cream - Topical | 4.6 % / W/W | 6/16/2010 |
SHEER TOUCH TOUCHER SOYEUX OIL-FREE SUNSCREEN ÉCRAN SOLAIRE SANS HUILE SPF/FPS 50+ | edgewell personal care canada, ulc | 02454572 | Lotion - Topical | 6 % | 10/6/2016 |
OLAY COMPLETE 15 UVA/UVB 365 DAILY MOISTURIZING LOTION WITH SPF BROAD SPECTRUM SPF 15 COMBINATION/OILY | procter & gamble inc | 02461269 | Lotion - Topical | 2.6 % | 10/1/2017 |
OLAY DEFINITY REFINING LOTION WITH UV PROTECTION | procter & gamble inc | 02270587 | Lotion - Topical | 1 % | 7/27/2006 |
OLAY PROFESSIONAL PRO-X AGE PROTECTION LOTION WITH SPF 30 | procter & gamble inc | 02310414 | Lotion - Topical | 2.25 % / W/W | 2/5/2009 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
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No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
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No UK EMC drug information found for this drug. |
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