EUCERIN OIL-CONTROL SPF 50 SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene lotion

Eucerin Oil-Control SPF 50 Sunscreen by

Drug Labeling and Warnings

Eucerin Oil-Control SPF 50 Sunscreen 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, Homosalate, Octisalate, Octocrylene

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 at least every 2 hours

■ use a water resistant sunscreen if swimming or sweating

■ 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

■ store this product in upright position

Inactive ingredients

Water, Alcohol Denat., Butyloctyl Salicylate, Silica, C12-15 Alkyl Benzoate, Polyglyceryl-6 Stearate, Sodium Stearoyl Glutamate, Diisostearoyl Polyglyceryl-3 Dimer Dilinoleate, Behenyl Alcohol, Butylene Glycol Dicaprylate/Dicaprate, Cetearyl Alcohol, Copernicia Cerifera (Carnauba) Wax, Dibutyl Adipate, L-Carnitine, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Tocopherol, Dimethicone, Silica Dimethyl Silylate, Diethylhexyl Syringylidenemalonate, Ethylcellulose, Glyceryl Behenate, Polyglyceryl-6 Octastearate, Phenoxyethanol, Glycerin, Xanthan Gum, Ethylhexylglycerin, Disodium EDTA, Hydroxyacetophenone, Polyglyceryl-6 Behenate, Cetyl Alcohol, Sodium Ascorbyl Phosphate

Questions?

1-800-227-4703

PRINCIPAL DISPLAY PANEL

Eucerin ®

Oil Control

+Oil Absorbing Minerals

Lightweight Sunscreen Lotion For Fact

50 Broad Spectrum SPF 50

Won't Clog Pores

Hypoallergenic | Fragrance Free

No Oxybenzone & Octinoxate

5 AOX SHIELD

Antioxidant Defense

Developed With Dermatologists

2.5 FL OZ (75 mL)

INGREDIENTS AND APPEARANCE

EUCERIN OIL-CONTROL SPF 50 SUNSCREEN 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66800-6000
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
LEVOCARNITINE (UNII: 0G389FZZ9M)
ENOXOLONE (UNII: P540XA09DR)
GLYCYRRHIZA ECHINATA ROOT (UNII: V6E722P1VB)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
POLYGLYCERYL-6 BEHENATE (UNII: 4T2L7QI313)
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
COPERNICIA PRUNIFERA WHOLE (UNII: 6EKZ38572S)
ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
DIBUTYL ADIPATE (UNII: F4K100DXP3)
TOCOPHEROL (UNII: R0ZB2556P8)
DIMETHICONE (UNII: 92RU3N3Y1O)
EDETATE SODIUM (UNII: MP1J8420LU)
ALCOHOL (UNII: 3K9958V90M)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
XANTHAN GUM (UNII: TTV12P4NEE)
POLYGLYCERYL-6 STEARATE (UNII: ETY9Q81E2T)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
DOCOSANOL (UNII: 9G1OE216XY)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
ETHYLHEXYLGLYCERYL BEHENATE (UNII: JRY34LRD7B)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIISOSTEAROYL POLYGLYCERYL-3 DIMER DILINOLEATE (UNII: G3232Z5S2O)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66800-6000-1	75 g in 1 TUBE; Type 0: Not a Combination Product	11/03/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/03/2021

Labeler - Beiersdorf Inc (001177906)