EUCERIN ADVANCED HYDRATION SUNSCREEN SPF 30 (- to deliver avobenzone 3%, homosalate 7%, octisalate 4.5%, octocrylene 8% aerosol, spray

Eucerin Advanced Hydration Sunscreen SPF 30 by

Drug Labeling and Warnings

Eucerin Advanced Hydration Sunscreen SPF 30 by is a Otc medication manufactured, distributed, or labeled by Beiersdorf Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

(To Deliver) Avobenzone 3%, Homosalate 7%, Octisalate 4.5%, Octocrylene 8%

Purpose

Sunscreen

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
Flammable: Do not use near heat, flame, or while smoking

DO NOT USE

Do not use on damaged or broken skin

WHEN USING

■ keep away from face to avoid breathing it

■ keep out of eyes. Rinse with water to remove.

■ use only as directed. Intentional misuse by deliberately concentrating and inhaling
the contents can be harmful or fatal.

■ do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.

STOP USE

Stop use and ask a doctor if rash occurs

KEEP OUT OF REACH OF CHILDREN

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

Directions

■ shake well before each use

■ spray liberally and spread evenly by hand 15 minutes before sun exposure

■ hold container 4 to 6 inches from the skin to apply

■ do not spray directly into face. Spray on hands then apply to face.

■ do not apply in windy conditions

■ use in a well-ventilated area

■ reapply:

■ after 80 minutes of swimming or sweating

■ immediately after towel drying

■ 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-sleeve shirts, pants, hats, and sunglasses

■ children under 6 months: Ask a doctor

Other information

■ protect this product from excessive heat and direct sun

■ store between 20° to 25°C (68° to 77°F)

■ may stain or damage some fabrics or surfaces

Inactive ingredients

Water, Dimethyl Ether, C12-15 Alkyl Benzoate, Neopentyl Glycol Diheptanoate, Butylene Glycol, Styrene/Acrylates Copolymer, Diethylhexyl Syringylidenemalonate, VP/Eicosene Copolymer, Glycyrrhetinic Acid, Glycyrrhiza Inflata Root Extract, Sodium Hyaluronate, Tocopherol (Vitamin E), Sodium Ascorbyl Phosphate, Hydroxyacetophenone, Aloe Barbadensis Leaf Juice, 1,2-Hexandiol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Potassium Hydroxide

Questions?

1-800-227-4703

PRINCIPAL DISPLAY PANEL

Eucerin ®

Advanced Hydration

+ Hyaluraonic Acid & Humenctants

Lightweight Sunscreen Lotion Spray

30

Broad Spectrum SPF 30

Hypoallergenic | Fragrance & Alcohol Free

No Oxybenzone & Octinoxante

5 AOX Shield Antioxidant Defense

Developed with Dermatologists

Water Resistant (80 Minutes)

INGREDIENTS AND APPEARANCE

EUCERIN ADVANCED HYDRATION SUNSCREEN SPF 30 
(to deliver) avobenzone 3%, homosalate 7%, octisalate 4.5%, octocrylene 8% aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66800-0376
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	7 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	8 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
ALLANTOIN GLYCYRRHETINIC ACID (UNII: H6FL381368)
TOCOPHEROL (UNII: R0ZB2556P8)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
WATER (UNII: 059QF0KO0R)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
DIMETHYL ETHER (UNII: AM13FS69BX)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)

Product Characteristics
Color	white (clear to white)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66800-0376-6	170 g in 1 CAN; Type 0: Not a Combination Product	03/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/30/2023

Labeler - Beiersdorf Inc (001177906)