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

Eucerin Daily Protection Face by

Drug Labeling and Warnings

Eucerin Daily Protection Face by is a Otc medication manufactured, distributed, or labeled by Beiersdorf Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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

PURPOSE

Purpose
Sunscreens

INDICATIONS & USAGE

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

Warnings
For external use only

DO NOT USE

Do not use on damaged or broken skin

WHEN USING

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

STOP USE

Stop use and ask a doctor if irritation occurs

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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 INGREDIENT

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

Questions or comments

1-800-227-4703

PRINCIPAL DISPLAY PANEL

Eucerin

Daily Protection
Face Lotion

Broad Spectrum SPF 30
Sunscreen

Moisturizes and helps protect skin against dailu UV exposure

Fragrance free

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10356-323
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42)	ENSULIZOLE	2 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.4 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	4.8 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10356-323-04	30 mL in 1 TUBE; Type 0: Not a Combination Product	08/12/2015
2	NDC: 10356-323-25	5 mL in 1 TUBE; Type 0: Not a Combination Product	08/12/2015
3	NDC: 10356-323-27	4 mL in 1 PACKET; Type 0: Not a Combination Product	08/12/2019
4	NDC: 10356-323-11	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/12/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	08/12/2015

Labeler - Beiersdorf Inc (001177906)