MedPath

Octisalate

Generic Name
Octisalate
Brand Names
Eucerin, Meijer, Sumadan Wash
Drug Type
Small Molecule
Chemical Formula
C15H22O3
CAS Number
118-60-5
Unique Ingredient Identifier
4X49Y0596W

Overview

Also known as Ethylhexyl Salicylate. Octyl salicylate is an oil soluble chemical sunscreen agent that absorbs UVB radiation. It does not protect against UVA. Octyl salicylate is used to augment the UVB protection in a sunscreen. Salicylates are weak UVB absorbers and they are generally used in combination with other UV filters. Octyl salicylate appears to have a good safety profile. It covers wavelength in the range 295-315 nm, peak at 307-310 nm. It is an ester of salicylic acid and 2-ethylhexanol. The salicylate portion of the molecule absorbs ultraviolet light to protect skin from the harmful effects of exposure to sunlight, while the ethylhexanol portion functions as an emollient.

Indication

Ingredient in sunscreens for protection against damage effects of sun light, provides protection from sunburns, aging and skin cancer.

Associated Conditions

  • Sunburn

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

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
50 mg in 1 g
7/1/2025
Andalou naturals
55560-0107
TOPICAL
50 mg in 1 mL
6/9/2025
Kenvue Brands LLC
69968-0828
TOPICAL
50 mg in 1 mL
7/1/2025
The Procter & Gamble Manufacturing Company
84126-153
TOPICAL
4.5 g in 100 g
6/9/2025
LS Promotions Inc
72449-415
TOPICAL
0.3 g in 4.2 g
3/21/2025
BENOW BEAUTY INC
85550-001
TOPICAL
5 g in 100 mL
4/14/2025
Valu Merchandisers
63941-929
TOPICAL
50 mg in 1 g
7/7/2025
OL PHARMA TECH LLC. (Drs. Pharmacy)
80489-235
TOPICAL
5 g in 100 g
3/24/2025
BEL STAR SA
14141-405
TOPICAL
50 mg in 1 mL
4/28/2025
Kenvue Brands LLC
69968-0816
TOPICAL
50 mg in 1 g
7/1/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
BRIGHT BOOST MOISTURIZER SPF 30
johnson & johnson inc
02488116
Lotion - Topical
4 % / W/W
1/6/2020
BOTANICAL EFFECTS HYDRATE & PROTECT BROAD SPECTRUM SUNSCREEN SPF 30
mary kay cosmetics ltd
02401282
Lotion - Topical
4.5 % / W/W
N/A
SHEER TOUCH TOUCHER SOYEUX OIL-FREE SUNSCREEN ÉCRAN SOLAIRE SANS HUILE SPF/FPS 50+
edgewell personal care canada, ulc
02454572
Lotion - Topical
4.5 %
10/6/2016
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
LIFTACTIV SPECIALIST FPS/SPF 30
vichy canada
02498642
Cream - Topical
5 % / W/W
3/24/2021
ROSALIAC UV LEGERE
laboratoires la roche-posay canada
02330792
Cream - Topical
3.3 % / W/W
6/16/2010
OLAY COMPLETE 15 UVA/UVB 365 DAILY MOISTURIZING LOTION WITH SPF BROAD SPECTRUM SPF 15 COMBINATION/OILY
procter & gamble inc
02461269
Lotion - Topical
4.5 %
10/1/2017
SHEER LOTION SPF 45 BARE SKIN FEEL
vichy canada
02401924
Lotion - Topical
5 % / W/W
4/8/2013
OLAY DEFINITY REFINING LOTION WITH UV PROTECTION
procter & gamble inc
02270587
Lotion - Topical
4 %
7/27/2006
LIFE BRAND SUNTHERA 3 SPF/FPS 15
fruit of the earth, inc
02290685
Lotion - Topical
4.0 %
4/9/2007

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
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
No UK EMC drug information found for this drug.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.