MedPath

Homosalate

Generic Name
Homosalate
Brand Names
Meijer
Drug Type
Small Molecule
Chemical Formula
C16H22O3
CAS Number
118-56-9
Unique Ingredient Identifier
V06SV4M95S

Overview

Homosalate is an organic compound that belongs to salicylates. It is an ester formed from salicylic acid and 3,3,5-trimethylcyclohexanol, a derivative of cyclohexanol. Salicylates prevent direct skin exposure to the sun’s harmful rays by absorbing ultraviolet (UV) light. Homosalate specifically absorbs short-wave UVB rays, which are associated with DNA damage and increased risk of skin cancer. It is a common ingredient in many commercially available sunscreens. There are no reported adverse effects from homosalate.

Indication

As ingredient in many sunscreen for protection against sunburn, skin 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
100 mg in 1 g
7/1/2025
Kenvue Brands LLC
69968-0828
TOPICAL
135 mg in 1 mL
7/1/2025
The Procter & Gamble Manufacturing Company
84126-153
TOPICAL
9 g in 100 g
6/9/2025
BENOW BEAUTY INC
85550-001
TOPICAL
7 g in 100 mL
4/14/2025
Valu Merchandisers
63941-929
TOPICAL
150 mg in 1 g
7/7/2025
OL PHARMA TECH LLC. (Drs. Pharmacy)
80489-235
TOPICAL
10 g in 100 g
3/24/2025
Kenvue Brands LLC
69968-0816
TOPICAL
150 mg in 1 g
7/1/2025
Rite Aid
11822-0941
TOPICAL
100 mg in 1 g
6/9/2025
Kenvue Brands LLC
69968-0702
TOPICAL
150 mg in 1 mL
7/1/2025
Murad, LLC
70381-131
TOPICAL
7 g in 100 mL
3/26/2025

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
BULL FROG WATER ARMOR SPORT QUICK SPRAY SUNSCREEN BROAD SPECTRUM SPF 50
sun & skin care research inc
02411113
Spray - Topical
10 % / W/W
N/A
BROAD SPECTRUM SPF 30 SPORT SUNSCREEN CONTINUOUS SPRAY
prime enterprises, llc
02397978
Spray, Bag-On-Valve - Topical
7.5 % / W/W
8/19/2013
BOTANICAL EFFECTS HYDRATE & PROTECT BROAD SPECTRUM SUNSCREEN SPF 30
mary kay cosmetics ltd
02401282
Lotion - Topical
5.0 % / W/W
N/A
BRIGHT BOOST MOISTURIZER SPF 30
johnson & johnson inc
02488116
Lotion - Topical
5 % / W/W
1/6/2020
SHEER TOUCH TOUCHER SOYEUX OIL-FREE SUNSCREEN ÉCRAN SOLAIRE SANS HUILE SPF/FPS 50+
edgewell personal care canada, ulc
02454572
Lotion - Topical
9 %
10/6/2016
LIFTACTIV SPECIALIST FPS/SPF 30
vichy canada
02498642
Cream - Topical
5 % / W/W
3/24/2021
LIFE BRAND SUNTHERA 3 SPF/FPS 15
fruit of the earth, inc
02290685
Lotion - Topical
3.0 %
4/9/2007
OLAY COMPLETE 15 UVA/UVB 365 DAILY MOISTURIZING LOTION WITH SPF BROAD SPECTRUM SPF 15 COMBINATION/OILY
procter & gamble inc
02461269
Lotion - Topical
4 %
10/1/2017
LIFE BRAND KIDS SUNSCREEN LOTION SPF 50+
fruit of the earth, inc
02497727
Lotion - Topical
13 % / W/W
4/20/2021
SHEER LOTION SPF 45 BARE SKIN FEEL
vichy canada
02401924
Lotion - Topical
10 % / W/W
4/8/2013

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.