Label: DAILY MOISTURIZER- lotion lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 24, 2024

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  • Active Ingredient

    Dimethicone 1.2%

  • Purpose

    Skin Protectant

  • Uses

    • Helps prevent and temporarily protects chafted, chapped or cracked skin.
    • Helps protect from the drying effects of wind and cold weather.
  • Warnings

    For external use only.

    When using this product

    • do not get into eyes

    Stop use and ask a doctor if

    • Condition worsens
    • Symptoms lasts more than 7 days or clear up and occur again with a few days.

    Do not use on

    • Deep or puncture wounds
    • animal bites
    • serious burns

    Keep out of reach of children

    If swallowed, get medical help or contact Poison Control Center right away.

    Directions

    Apply as needed.

  • Inactive Ingredients

    Water (Aqua), Glycerin, Petrolatum, Isopropyl Palmatate, Distearyldimonium Chloride, Cetyl Alcohol, Avena Sativa (oat) kernel flour, Sodium Chloride, Sodium Hydroxide, Ethylhexylglycerin, Phenoxyethanol.

  • Questions or Comments?

    1-800-925-4733.

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    DAILY MOISTURIZER 
    lotion lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-5934
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE1.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)  
    OATMEAL (UNII: 8PI54V663Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-5934-0271 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/19/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/19/2023
    Labeler - Walgreens (008965063)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOLLO HEALTH AND BEAUTY CARE201901209manufacture(0363-5934)
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