Label: DAILY MOISTURIZING- dimethicone lotion

  • NDC Code(s): 72288-496-34, 72288-496-44
  • Packager: Amazon.com Services LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 10, 2023

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  • Active ingredient

    Dimethicone 1.2%

  • Purpose

    Skin protectant

  • Uses

    • helps prevent and temporarily protects chafed, 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 last more than 7 days or clear up and occur again within 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 a Poison Control Center right away.

  • Directions

    apply as needed

  • Inactive ingredients

    water, glycerin, distearyldimonium chloride, petrolatum, isopropyl palmitate, cetyl alcohol, Avena sativa (oat) kernel flour, benzyl alcohol, sodium chloride, sodium hydroxide

  • SPL UNCLASSIFIED SECTION

    DISTRIBUTED BY: Amazon.com Services, Inc.

    Seattle, WA 98109

    1-877-485-0385

    (c) Amazon.com, Inc., or its affiliates.  All rights reserved.  Solimo and all related logos are trademarks of Amazon.com, Inc. or its affiliates.

    496.000/496AA/619AC rev 2

  • principal display panel

    SOLIMO

    Daily Baby Lotion

    SKIN PROTECTANT

    With colloidial oatmeal

    Peadiatrician tested

    18 FL OZ (532 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    DAILY MOISTURIZING  
    dimethicone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72288-496
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE12 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    OAT KERNEL OIL (UNII: 3UVP41R77R)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72288-496-44532 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/25/2018
    2NDC:72288-496-34227 g in 1 TUBE; Type 0: Not a Combination Product04/25/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34704/25/2018
    Labeler - Amazon.com Services LLC (128990418)
    Registrant - Vi Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, LLC790752542manufacture(72288-496)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, LLC088520668manufacture(72288-496)
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