Label: KIEHLS SINCE 1851 ULTRA FACIAL MELTDOWN RECOVERY- colloidal oatmeal cream

  • NDC Code(s): 49967-571-01, 49967-571-02, 49967-571-03, 49967-571-04, view more
    49967-571-05, 49967-571-06
  • Packager: L’Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 29, 2026

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  • Active ingredient

    Colloidal oatmeal 1%

  • Purpose

    Skin protectant

  • Uses

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

    • rashes
    • eczema
    • poison ivy, oak, or sumac
    • insect bites
  • 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 7days 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, glycerin, caprylic/capric triglyceride, squalane, butyrospermum parkii (shea) butter, stearyl alcohol, cetyl alcohol, myristyl myristate, C15-19 alkane, phenoxyethanol, panthenol, glyceryl stearate, dimethicone, PEG-100 stearate, persea gratissima (avocado) oil, chlorphenesin, stearic acid, palmitic acid, trisodium ethylenediamine disuccinate, carbomer, acrylates/C10-30 alkyl acrylate crosspolymer, tocopherol, bisabolol, zinc gluconate, glycine soja (soybean) oil, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, xanthan gum, ethylhexylglycerin, adenosine, sodium hydroxide, myristic acid, citric acid, helianthus annuus (sunflower) seed oil, rosmarinus officinalis (rosemary) leaf extract

  • Questions or comments?

    Call toll free 1-800-946-4453

  • PRINCIPAL DISPLAY PANEL

    image of 14 mL primary

  • PRINCIPAL DISPLAY PANEL

    image of 14 mL secondary

  • PRINCIPAL DISPLAY PANEL

    image of 28 mL primary

  • PRINCIPAL DISPLAY PANEL

    image of 28 mL bottom

  • PRINCIPAL DISPLAY PANEL

    image of 50 mL bottom

  • PRINCIPAL DISPLAY PANEL

    image of 50 mL primary

  • PRINCIPAL DISPLAY PANEL

    125 bottom125150

  • INGREDIENTS AND APPEARANCE
    KIEHLS SINCE 1851 ULTRA FACIAL MELTDOWN RECOVERY 
    colloidal oatmeal cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-571
    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
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)  
    SQUALANE (UNII: GW89575KF9)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    MYRISTYL MYRISTATE (UNII: 4042ZC00DY)  
    C15-19 ALKANE (UNII: CI87N1IM01)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    GLYCERYL STEARATE (UNII: 230OU9XXE4)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PERSEA GRATISSIMA (AVOCADO) OIL (UNII: 6VNO72PFC1)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
    CARBOMER (UNII: 0A5MM307FC)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    BISABOLOL (UNII: 24WE03BX2T)  
    ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ADENOSINE (UNII: K72T3FS567)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    MYRISTIC ACID (UNII: 0I3V7S25AW)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI)  
    ROSEMARY (UNII: IJ67X351P9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-571-011 in 1 CARTON11/15/2025
    114 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:49967-571-0228 mL in 1 JAR; Type 0: Not a Combination Product11/15/2025
    3NDC:49967-571-0350 mL in 1 JAR; Type 0: Not a Combination Product11/15/2025
    4NDC:49967-571-043 mL in 1 PACKET; Type 0: Not a Combination Product05/14/2026
    5NDC:49967-571-05125 mL in 1 JAR; Type 0: Not a Combination Product05/29/2026
    6NDC:49967-571-06150 mL in 1 POUCH; Type 0: Not a Combination Product05/29/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01611/15/2025
    Labeler - L’Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'OREAL USA, INC.185931458manufacture(49967-571) , pack(49967-571)
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