EUCERIN DAILY PROTECTION FACE- ensulizole, octinoxate, octisalate, titanium dioxide, zinc oxide lotion 
Beiersdorf Inc

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Eucerin Daily Protection Face

Active ingredients
Ensulizole 2%
Octinoxate 7.5%
Octisalate 4.5%
Titanium Dioxide 2.4%
Zinc Oxide 4.8%

Purpose
Sunscreens

Uses
• helps prevent sunburn • if used as directed with other sun protection
measures (see Directions), decreases the risk of skin cancer and early skin aging
caused by the sun.

Warnings
For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes.
Rinse with water to remove

Stop use and ask a doctor if irritation occurs

Keep out of reach of children. If swallowed,
get medical help or contact a Poison Control
Center right away.

Directions
For sunscreen use: • apply liberally 15
minutes before sun exposure • use a water
resistant sunscreen if swimming or sweating
• reapply at least every 2 hours
Sun Protection Measures. Spending time in
the sun increases your risk of skin cancer and
early skin aging. To decrease this risk regularly
use a sunscreen with a Broad Spectrum SPF
value of 15 or higher and other sun protection
measures including:
• limit time in the sun, especially from
10 a.m.-2 p.m.• wear long-sleeved shirts,
pants, hats, and sunglasses.
• Children under 6 months of age: Ask a doctor

Inactive Ingredients

Water, Glycerin, C12-15 Alkyl Benzoate,

Dimethicone, Cyclomethicone, Methylpropanediol,

Cetearyl Alcohol, Cetyl Alcohol, Ceteareth-20,

Phenoxyethanol, Glyceryl Stearate SE, Sodium

Lactate, Lactic Acid, 1,2-Hexanediol,

Hydrogenated Coco-Glycerides,

VP/Hexadecene Copolymer, Xanthan Gum,

PEG-40 Castor Oil, Sodium Hydroxide,

Trisodium EDTA, Alumina, Sodium Cetearyl

Sulfate, Triethoxycaprylylsilane, Simethicone

Questions or comments

1-800-227-4703

Eucerin

Face

Gentle Protection Daily Lotion

Broad Spectrum SPF 30 Sunscreen

Provides 24 hour Moisture and helps

defend against sun damage

UV filter Blend

Dermatologist Recommended Brand

eucdpface front

eucdpfaceback

EUCERIN DAILY PROTECTION FACE 
ensulizole, octinoxate, octisalate, titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10356-323
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE2 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.5 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE2.4 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE4.8 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CYCLOMETHICONE (UNII: NMQ347994Z)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
LACTIC ACID (UNII: 33X04XA5AT)  
COCO-GLYCERIDES (UNII: ISE9I7DNUG)  
POLYOXYL 40 CASTOR OIL (UNII: 4ERD2076EF)  
SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)  
XANTHAN GUM (UNII: TTV12P4NEE)  
EDETATE TRISODIUM (UNII: 420IP921MB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)  
TRIMETHOXYCAPRYLYLSILANE (UNII: FZ07E4LW2M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10356-323-0430 mL in 1 TUBE; Type 0: Not a Combination Product08/12/2015
2NDC:10356-323-255 mL in 1 TUBE; Type 0: Not a Combination Product08/12/2015
3NDC:10356-323-274 mL in 1 PACKET; Type 0: Not a Combination Product08/12/2019
4NDC:10356-323-11118 mL in 1 BOTTLE; Type 0: Not a Combination Product08/12/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02008/12/2015
Labeler - Beiersdorf Inc (001177906)

Revised: 1/2024
Document Id: 22cfebba-d598-e758-e063-6394a90a1e1b
Set id: 76403f03-aee9-4c0b-b331-f79b6953118c
Version: 9
Effective Time: 20240101
 
Beiersdorf Inc