Label: NEUREXA- colloidal oatmeal cream

  • NDC Code(s): 87110-004-01, 87110-004-02
  • Packager: METHODIQ INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 3, 2026

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  • Active ingredient

    Colloidal Oatmeal 1%

  • Purpose

    Active ingredients: Colloidal Oatmeal 1%

    Purpose: Skin Protectant

  • Uses

    Temporarily protects and helps relieve minor skin irritation and itching due to:

    • rashes

    • eczema

  • Warnings

    For external use only.

    When using this product

    • do not get into eyes

    Stop use and ask a doctor if

    • condition worsens

    • symptoms last more than 7 days or clear up and occur again within a few days

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

  • Directions

    Apply as needed

  • Inactive ingredients

    Water, Dimethyl

    Isosorbide, Caprylic/

    Capric Triglyceride,

    Isopropyl Myristate,

    Glycerin, Glyceryl Stearate

    Citrate, Butyrospermum

    Parkii (Shea) Butter,

    Methylpropanediol,

    Hydroxyethyl

    Acrylate/Sodium

    Acryloyldimethyl Taurate

    Copolymer, Butylene

    Glycol, Polyglyceryl-3

    Stearate, Isopropyl

    Isostearate, Niacinamide,

    Squalane, Pentylene

    Glycol, Hydrogenated

    Lecithin, Bis-Diglyceryl

    Polyacyladipate-2,

    Hydrolyzed Vegetable

    Protein, Isosorbide

    Dicaprylate, Polyglyceryl-4

    Caprate, Simmondsia

    Chinensis (Jojoba) Seed

    Oil, Saccharomyces

    Ferment, Propanediol,

    Stearyl Glycyrrhetinate,

    Trehalose, Allantoin,

    Bisabolol, Madecassoside,

    Tocopherol, Caprylyl

    Glycol, Chlorphenesin,

    Sorbitan Isostearate,
    Aloe Barbadensis Leaf Extract,
    Dihydroxypropylamino Isobutyphenyl Benzylbenzamide,
    Disodium EDTA,
    Sodium Hyaluronate,
    Sodium Carboxymethyl Beta-Glucan,
    Ethylhexylglycerin,
    Helianthus Annuus (Sunflower) Seed Oil,
    Lauroyl Lysine,
    Hydroxyphenyl Propamidobenzoic Acid,
    Sodium Lauroyl Lactylate,
    Sodium Benzoate,
    Zingiber Officinale (Ginger) Root Extract,
    Ascorbyl Palmitate,
    Ceramide NP,
    Phenoxyethanol,
    Ceramide AP,
    Phytosphingosine,
    Cholesterol,
    Xanthan Gum,
    Carbomer,
    Ceramide EOP.

  • PRINCIPAL DISPLAY PANEL

    30ml 1.0 Fl. Oz.

    Neurexa

    Eczema Relief

    1

    2

  • INGREDIENTS AND APPEARANCE
    NEUREXA 
    colloidal oatmeal cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87110-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    TREHALOSE (UNII: B8WCK70T7I)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)  
    BISABOLOL (UNII: 24WE03BX2T)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    GINGER (UNII: C5529G5JPQ)  
    HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885)  
    ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)  
    SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
    METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
    HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)  
    ISOSORBIDE DICAPRYLATE (UNII: 0IK29C4889)  
    CERAMIDE NP (UNII: 4370DF050B)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CERAMIDE AP (UNII: F1X8L2B00J)  
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CHOLESTEROL (UNII: 97C5T2UQ7J)  
    CERAMIDE 1 (UNII: 5THT33P7X7)  
    SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)  
    BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    LAUROYL LYSINE (UNII: 113171Q70B)  
    ASCORBYL PALMITATE (UNII: QN83US2B0N)  
    CARBOMER (UNII: 0A5MM307FC)  
    MADECASSOSIDE (UNII: CQ2F5O6YIY)  
    ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)  
    SODIUM CARBOXYMETHYL .BETA.-GLUCAN (DS 0.65-0.85) (UNII: 2YGO1190AP)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ALLANTOIN (UNII: 344S277G0Z)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
    CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    SQUALANE (UNII: GW89575KF9)  
    GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)  
    POLYGLYCERYL-3 STEARATE (UNII: 8FDA8C98S3)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87110-004-011 in 1 CARTON02/01/2026
    130 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:87110-004-021 in 1 CARTON02/01/2026
    250 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01602/01/2026
    Labeler - METHODIQ INC. (119377051)
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