EUCERIN ADVANCE HYDRATION SUNSCREEN SPF 30- avobenzone, homosalate, octisalate, octocrylene lotion

Eucerin Advance Hydration Sunscreen SPF 30 by

Drug Labeling and Warnings

Eucerin Advance 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

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

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 product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ apply liberally 15 minutes before sun exposure

■ 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

■ may stain or damage some fabrics or surfaces

Inactive ingredients

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

Questions?

1-800-227-4703

PRINCIPAL DISPLAY PANEL

Eucerin ®

Advanced Hydration

+Hyaluronic Acid & Humectants

Lightweight Sunscreen Lotion

30 Broad Spectrum SPF 30

Hypoallergenic | Fragrance Free

No Oxybenzone & Octinoxate

5 AOX Shield™

Antioxidant Defense

Developed with Dermatologists

Water Resistant (80 Minutes)

5 FL OZ (150 mL)

INGREDIENTS AND APPEARANCE

EUCERIN ADVANCE HYDRATION SUNSCREEN SPF 30 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66800-3000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	8 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ)
ENOXOLONE (UNII: P540XA09DR)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TOCOPHEROL (UNII: R0ZB2556P8)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)

Product Characteristics
Color	white (White to off-white)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66800-3000-1	150 g in 1 TUBE; Type 0: Not a Combination Product	12/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/01/2021

Labeler - Beiersdorf Inc (001177906)