Label: EUCERIN DAILY HYDRATION- avobenzone, homosalate, octisalate, octocrylene cream
- NDC Code(s): 10356-335-34
- 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
• 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, Tapioca Starch, Butylene Glycol, Cetyl Alcohol,
Hydrogenated Cocoglycerides, Myristyl Myristate, Stearyl Alcohol, Palmitic Acid,
Glyceryl Stearate, Stearic Acid, Glycyrrhiza Inflata Root Extract, Dimethicone,
1,2-Hexanediol, Phenoxyethanol, Silica Dimethyl Silylate, Decylene Glycol,
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzyl Alcohol, Xanthan Gum,
Sodium Hydroxide, Trisodium EDTA.
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INGREDIENTS AND APPEARANCE
EUCERIN DAILY HYDRATION
avobenzone, homosalate, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10356-335 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 5 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 9 g in 100 g Inactive Ingredients Ingredient Name Strength SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE TRISODIUM (UNII: 420IP921MB) HYDROGENATED COCO-GLYCERIDES (UNII: XDD37N2GPR) MYRISTYL MYRISTATE (UNII: 4042ZC00DY) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) PALMITIC ACID (UNII: 2V16EO95H1) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) STEARIC ACID (UNII: 4ELV7Z65AP) DIMETHICONE (UNII: 92RU3N3Y1O) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) DECYLENE GLYCOL (UNII: S57M60MI88) XANTHAN GUM (UNII: TTV12P4NEE) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) PHENOXYETHANOL (UNII: HIE492ZZ3T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) BENZYL ALCOHOL (UNII: LKG8494WBH) STARCH, TAPIOCA (UNII: 24SC3U704I) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10356-335-34 226 g in 1 TUBE; Type 0: Not a Combination Product 08/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/01/2016 Labeler - Beiersdorf Inc (001177906)