Label: EUCERIN ECZEMA RELIEF HAND- oatmeal cream
- NDC Code(s): 10356-375-25, 10356-375-28
- Packager: Beiersdorf Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 30, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- WARNINGS
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- QUESTIONS
- PURPOSE
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INACTIVE INGREDIENT
Inactive Ingredients
Water, Glycerin, Mineral Oil, Cetyl Alcohol, Glyceryl Stearate, Stearyl Alcohol, Hydrogenated Coco-Glycerides, Caprylic/Capric Triglyceride, Octyldodecanol, Butyrospermum Parkii (Shea) Butter, Cetyl Palmitate, PEG-40 Stearate, Glycyrrhiza Inflata Root Extract, Ceramide NP, Phenoxyethanol, Caprylyl Glycol, Benzyl Alcohol, Decylene Glycol, Menthoxypropanediol, Sodium Citrate, Citric Acid.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EUCERIN ECZEMA RELIEF HAND
oatmeal creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10356-375 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL 1 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) MINERAL OIL (UNII: T5L8T28FGP) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) OCTYLDODECANOL (UNII: 461N1O614Y) CETYL PALMITATE (UNII: 5ZA2S6B08X) PEG-40 STEARATE (UNII: ECU18C66Q7) GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ) CERAMIDE 3 (UNII: 4370DF050B) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) BENZYL ALCOHOL (UNII: LKG8494WBH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH) DECYLENE GLYCOL (UNII: S57M60MI88) SHEA BUTTER (UNII: K49155WL9Y) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) HYDROGENATED COCO-GLYCERIDES (UNII: XDD37N2GPR) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10356-375-28 78 g in 1 TUBE; Type 0: Not a Combination Product 06/01/2017 2 NDC:10356-375-25 5 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 06/01/2017 Labeler - Beiersdorf Inc (001177906)