Label: ECZEMA RELIEF CREAM BODY WASH- oatmeal lotion
- NDC Code(s): 10356-382-26
- 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
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INACTIVE INGREDIENT
Inactive Ingredients
Water, Isopropyl Palmitate, Glycerin,
Cetearyl Alcohol, Sodium
Cocoamphoacetate, Caprylic/Capric
Triglyceride, Octyldodecanol,
C12-15 Alkyl Benzoate, Sodium
Myreth Sulfate, Cetearyl
Isononanoate, Xanthan Gum,
Ceramide NP, Alanine, Arginine HCl,
Carnitine, Glycine, Sodium PCA,
Lauryl Glucoside, Citric Acid,
Sodium Chloride, Phenoxyethanol,
Carbomer, Sodium Hydroxide,
Pentylene Glycol, Decylene Glycol,
Sodium Benzoate. - PURPOSE
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PRINCIPAL DISPLAY PANEL
Eucerin
Eczema Relief Cream & Body Wash
Eczema Prone Skin
Gentle cream and non-foaming body wash
to help calm dry, itchy skin
associated with eczemaColloidal Oatmeal Skin Protectant Cream
and Body Wash
Fragrance, Dye & Soap Free
Dermatological Skincare
Eucerin Dermatologist Recommended
Eucerin Baby
Eczema Relief Cream & Body Wash
Eczema Prone Skin
Gentle cream and non-foaming body wash
to help calm dry, itchy skin
associated with eczemaColloidal Oatmeal Skin Protectant Cream
and Body Wash
Fragrance, Dye & Soap Free
Dermatological Skincare
Eucerin Dermatologist Recommended
-
INGREDIENTS AND APPEARANCE
ECZEMA RELIEF CREAM BODY WASH
oatmeal lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10356-382 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL 2 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674) SODIUM CHLORIDE (UNII: 451W47IQ8X) DECYLENE GLYCOL (UNII: S57M60MI88) SODIUM HYDROXIDE (UNII: 55X04QC32I) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) PENTYLENE GLYCOL (UNII: 50C1307PZG) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CETEARYL ISONONANOATE (UNII: P5O01U99NI) XANTHAN GUM (UNII: TTV12P4NEE) GLYCINE (UNII: TE7660XO1C) CARBOMER 980 (UNII: 4Q93RCW27E) SODIUM MYRETH SULFATE (UNII: 2VLC033A4E) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y) CARNITINE (UNII: S7UI8SM58A) SODIUM BENZOATE (UNII: OJ245FE5EU) OCTYLDODECANOL (UNII: 461N1O614Y) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CERAMIDE 3 (UNII: 4370DF050B) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ALANINE (UNII: OF5P57N2ZX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10356-382-26 400 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 07/01/2022 Labeler - Beiersdorf Inc (001177906)