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Sulisobenzone

Generic Name
Sulisobenzone
Drug Type
Small Molecule
Chemical Formula
C14H12O6S
CAS Number
4065-45-6
Unique Ingredient Identifier
1W6L629B4K

Overview

Sulisobenzone is approved by the FDA in concentrations of up to 10% and in Canada, is approved by Health Canada at the same concentrations . It works to filter out both UVA and UVB rays, protecting the skin from sun UV damage . The UV-filter substance, sulisobenzone (BP-4) is widely used an ingredient in sunscreens and other personal care products , . It falls under the drug category of benzophenones. The benzophenones are a group of aromatic ketones that have both pharmaceutical and industrial applications . Benzophenones may be found organically in fruits such as grapes . Benzophenones are used as photoinitiators, fragrance enhancers, ultraviolet curing agents, and, occasionally, as flavor ingredients; they are also used in the manufacture of insecticides, agricultural chemicals, and pharmaceuticals and as an additive for plastics, coatings, and adhesives . As a group, benzophenones may be used to delay photodegradation or extend shelf life in toiletries and plastic surface coatings .

Indication

Sunscreening agents are used to prevent sunburn, actinic keratosis, and premature skin aging and to reduce the incidence of skin cancer .

Associated Conditions

No associated conditions information available.

Clinical Trials

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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
No FDA approvals found for this drug.

EMA Drug Approvals

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

HSA Drug Approvals

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Manufacturer
Approval Number
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Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

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

PPB Drug Approvals

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

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
SEBAMED SUN LOTION SPF 8
lofco canada inc.
02240488
Lotion - Topical
1 %
4/17/2000
SUNSCREEN SPF 24
vagheggi s.p.a.
02242035
Cream - Topical
1 %
5/15/2000
HYDRA LIFE FLUIDE PRO-JEUNESSE AVEC PROTECTION UVA/UVB
parfums christian dior
02347504
Emulsion - Topical
1.5 % / W/W
12/22/2011
SEBAMED SUN CREAM SPF 16
lofco canada inc.
02240486
Cream - Topical
1.00 %
4/17/2000
HYDRACTION VISIBLE DEFENSE CREME RICHE HYDRA-PROTECTRICE SPF 20
parfums christian dior
02294907
Emulsion - Topical
0.5 %
5/5/2007
HAWAIIAN TROPIC HERBAL PROTECTIVE GEL 15 SPF
tanning research laboratories, inc.
02230341
Gel - Topical
0.1 %
4/4/1997
SEBAMED SUN CREAM SPF 8
lofco canada inc.
02240482
Cream - Topical
1.00 %
4/17/2000
HYDRACTION VISIBLE DEFENSE CREME LEGERE HYDRA-PROTECTRICE SPF 20
parfums christian dior
02294893
Emulsion - Topical
0.5 %
5/5/2007
UHA AFTER WAX MOISTURIZING LOTION SPF 15
ubermed incorporated
02243583
Lotion - Topical
3 %
N/A
HYDRA LIFE CRÈME PRO-JEUNESSE AVEC PROTECTION UVA/UVB
parfums christian dior
02347490
Cream - Topical
1.0 % / W/W
12/22/2011

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.

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