MedPath

Titanium dioxide

Generic Name
Titanium dioxide
Brand Names
Eucerin
Drug Type
Small Molecule
Chemical Formula
O2Ti
CAS Number
13463-67-7
Unique Ingredient Identifier
15FIX9V2JP

Overview

Titanium dioxide, also known as titanium(IV) oxide or titania, is the naturally occurring oxide of titanium. It is used as a pigment under the names titanium white, Pigment White 6 (PW6), or CI 77891. It is typically extracted from ilmenite, rutile and anatase.

Indication

Titanium dioxide is used in most sunscreens to block UVA and UVB rays, similar to zinc oxide.

Associated Conditions

  • Atopic Dermatitis
  • Blisters
  • Sunburn
  • Wound
  • Abrasions
  • Dry, cracked skin

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
SKIN BOSS L.L.C.
85503-202
TOPICAL
80 mg in 1 g
5/21/2025
Hello Bello
73418-106
TOPICAL
80 mg in 1 g
5/14/2025
Crown Laboratories
0316-2046
TOPICAL
89.6 mg in 1 mL
5/20/2025
NEXTEX CORPORATION
85575-210
TOPICAL
30 mg in 1 g
5/22/2025
Brent Loftis, D.O., Inc., A California Medical Corporation
85334-212
TOPICAL
40 mg in 1 g
5/20/2025
CLEARLY BEAUTIFUL SKIN AND ACNE CLINIC LLC
85493-203
TOPICAL
80 mg in 1 g
5/22/2025
The Hain Celestial Group, Inc.
61995-1125
TOPICAL
7.0 g in 100 g
3/23/2011
Crown Laboratories
0316-2074
TOPICAL
90.4 mg in 1 mL
3/3/2025
BIO EARTH MANUFACTURING (PTY) LTD
70116-014
TOPICAL
8 g in 100 mL
5/28/2025
CLEARLY BEAUTIFUL SKIN AND ACNE CLINIC LLC
85493-201
TOPICAL
80 mg in 1 g
5/22/2025

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
VEELANZ'S OINTMENT
SIN16547P
OINTMENT
10.01% w/w
7/7/2022

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
C.T. FOUNDATION CREME FINISH SPF 15, SHADE: 4
la prairie inc.
02242858
Cream - Topical
15.8 G / 100 G
5/15/2001
LUMINOUS MOISTURIZING FOUNDATION SPF 15
act cosmetics america inc
02463342
Lotion - Topical
12.2 % / W/W
N/A
LIFE BRAND SUNTHERA 3 SPF/FPS 15
fruit of the earth, inc
02290685
Lotion - Topical
0.66 %
4/9/2007
SHISEDO ELX ESS.EML COMPACT SUNSC.REF.OC20
shiseido company ltd.
02099314
Powder - Topical
22.7 %
9/10/1996
SHISEIDO NATURAL MATTE FOUNDAT.(OIL-FREE)P2
shiseido company ltd.
02063417
Emulsion - Topical
11.1 %
12/31/1995
AQUA-FLUID
pierre fabre dermo-cosmetique canada inc
02522942
Emulsion - Topical
3.4 % / W/W
6/2/2022
LAIT PROTECTEUR HYDRO-SATINANT SPF15
lancome canada
02207575
Lotion - Topical
2.5 %
12/31/1996
BANANA BOAT BABY BLOCK SUNBLOCK LOTION SPF 50
playtex ltd.
02242584
Lotion - Topical
1.4 %
2/25/2002
BOBBI BROWN SKIN FOUNDATION CUSHION COMPACT SPF 35 PROTECT & RECHARGE
dist. bobbi brown professional cosmetics
02453886
Lotion - Topical
4.2 % / W/W
9/15/2016
A M HAND CREAM SPF 15
la prairie inc.
02241020
Cream - Topical
5 %
8/30/2000

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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