Label: EUCERIN REDNESS RELIEF DAILY PERFECTING- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 10356-353-05, 10356-353-32
- Packager: Beiersdorf Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 29, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
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. -
INACTIVE INGREDIENT
Inactive ingredients
Water, Glycerin, Methylpropanediol, Titanium Dioxide,
Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol,
Pentylene Glycol, Dimethicone, Glycyrrhiza Inflata Root
Extract, Potassium Cetyl Phosphate, Caprylyl Glycol,
Acrylates/C10-30 Alkyl Acrylate Crosspolymer,
Xanthan Gum, Phenoxyethanol, Chromium Oxide
Greens, Sodium Hydroxide, Trisodium EDTA.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EUCERIN REDNESS RELIEF DAILY PERFECTING
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10356-353 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 4.5 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 3.5 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 3.5 g in 100 mL Inactive Ingredients Ingredient Name Strength PENTYLENE GLYCOL (UNII: 50C1307PZG) METHYLPROPANEDIOL (UNII: N8F53B3R4R) SHEA BUTTER (UNII: K49155WL9Y) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM HYDROXIDE (UNII: 55X04QC32I) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) EDETATE TRISODIUM (UNII: 420IP921MB) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ) XANTHAN GUM (UNII: TTV12P4NEE) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) CHROMIC OXIDE (UNII: X5Z09SU859) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10356-353-05 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/30/2017 2 NDC:10356-353-32 1.5 mL in 1 PACKET; Type 0: Not a Combination Product 03/30/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/30/2017 Labeler - Beiersdorf Inc (001177906)