Eucerin Redness Relief Daily Perfecting

Eucerin Redness Relief Daily Perfecting by

Drug Labeling and Warnings

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

Drug Details [pdf]

EUCERIN REDNESS RELIEF DAILY PERFECTING- octinoxate, octisalate, titanium dioxide lotion 
Beiersdorf Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Eucerin Redness Relief Daily Perfecting

Active ingredients
Octinoxate 7.5%
Octisalate 5.0%
Titanium Dioxide 4.0%

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

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.

Warnings
For external use only

Do not use on damaged or broken skin.

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

Stop use and ask a doctor if rash or irritation occurs.

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

Inactive ingredients
Water, Glycerin, Dimethicone, Polyglyceryl-3 Methylglucose Distearate, Butyrospermum Parkii
(Shea) Butter, Lauroyl Lysine, Squalane, Alcohol Denat., Sorbitan Stearate, Phenoxyethanol,
Butylene Glycol, Magnesium Aluminum Silicate, Glycyrrhiza Inflata Root Extract, Xanthan Gum,
Methylparaben, Ethylparaben, Iodopropynyl Butylcarbamate, Trimethoxycaprylylsilane,
Chromium Oxide Greens, Chromium Hydroxide Green, Ultramarines.

Eucerin

REDNESS RELIEF

DAY LOTION

Broad Spectrum SPF 15
Sunscreen eucrrcarton


Subtle Green Color Neutralizers

immediately reduce visible redness and blotchiness

Fragrance-free

EUCERIN REDNESS RELIEF DAILY PERFECTING 
octinoxate, octisalate, titanium dioxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 10356-352
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.5 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SHEA BUTTER (UNII: K49155WL9Y)  
LAUROYL LYSINE (UNII: 113171Q70B)  
SQUALANE (UNII: GW89575KF9)  
ALCOHOL (UNII: 3K9958V90M)  
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ)  
XANTHAN GUM (UNII: TTV12P4NEE)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
ETHYLPARABEN (UNII: 14255EXE39)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
TRIMETHOXYCAPRYLYLSILANE (UNII: FZ07E4LW2M)  
CHROMIC OXIDE (UNII: X5Z09SU859)  
ULTRAMARINE BLUE (UNII: I39WR998BI)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 10356-352-0550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/02/200901/31/2019
2NDC: 10356-352-321.5 mL in 1 PACKET; Type 0: Not a Combination Product01/02/200901/31/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35201/02/200907/01/2019
Labeler - Beiersdorf Inc (001177906)

Revised: 1/2020
 
Beiersdorf Inc