EUCERIN FACE IMMERSIVE HYDRATION- avobenzone, homosalate, octisalate, octocrylene lotion

Eucerin Face immersive Hydration by

Drug Labeling and Warnings

Eucerin Face immersive Hydration 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

Avobenzone 3%

Homosalate 10%

Octisalate 4.5%

Octocrylene 10%

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 rash 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

children under 6 months of age: Ask a doctor

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.

OTHER SAFETY INFORMATION

Other information

protect this product from excessive heat and direct sun

INACTIVE INGREDIENT

Inactive ingredients

Water, Alcohol Denat., Glycerin, Neopentyl
Glycol Diheptanoate, Dicaprylyl Carbonate,
Hydroxypropyl Starch Phosphate,
1,2-Hexanediol, Behenyl Alcohol, Cetearyl
Alcohol, Copernicia Cerifera (Carnauba) Wax,
Glyceryl Stearate, Propylheptyl Caprylate,
Tapioca Starch, Glycine Soja (Soybean)
Germ Extract, Glycyrrhetinic Acid, Sodium
Hyaluronate, Tocopherol, Sodium Stearoyl
Glutamate, Phenoxyethanol, Silica Dimethyl
Silylate, Disodium EDTA, Ethylhexylglycerin,
Xanthan Gum.

PRINCIPAL DISPLAY PANEL

Eucerin

Face

Immersive Hydration

Daily Lotion

Broad Spectrum SPF 30
Sunscreen

Hydrates skin and improves the look of fine lines and wrinkles

+ MULTI-WEIGHT HYALURONIC ACID + ANTIOXIDANT COMPLEX

INVISIBLE FINISH
DERMATOLOGIST RECOMMENDED BRAND

INGREDIENTS AND APPEARANCE

EUCERIN FACE IMMERSIVE HYDRATION 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10356-385
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	10 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
SOYBEAN GERM (UNII: JBW2VHD14M)
ALCOHOL (UNII: 3K9958V90M)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
CARNAUBA WAX (UNII: R12CBM0EIZ)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
STARCH, TAPIOCA (UNII: 24SC3U704I)
ENOXOLONE (UNII: P540XA09DR)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10356-385-16	1 in 1 CARTON	06/15/2023
1		75 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 10356-385-02	7 g in 1 TUBE; Type 0: Not a Combination Product	01/15/2024
3	NDC: 10356-385-05	1 in 1 CARTON	11/05/2024
3		50 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	06/15/2023

Labeler - Beiersdorf Inc (001177906)