Label: LUCKY DAILY MOISTURIZING- dimethicone lotion

  • NDC Code(s): 20276-044-08, 20276-044-12, 20276-044-18
  • Packager: Delta Brands Inc
  • 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 July 25, 2016

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Dimethicone 1%

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  • Purpose

    Skin protectant

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  • Uses

    ■Helps prevent and temporarily protects chafed, chapped, or cracked skin

    ■Helps prevent and protect from the drying effects of wind and cold weather

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  • Warnings

    For external use only

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  • When using this product

    ■Do not get into eyes

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  • 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.

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  • Do not use on

    ■Deep or puncture wounds

    ■Animal bites

    ■Serious burns

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  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center immediately.

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  • Directions

    Apply as needed

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  • Inactive ingredients

    avena sativa (oat) kernel flour, benzyl alcohol, carbomer, ceteareth-20, cetrimonium chloride, cetearyl alcohol, FD&C blue no.1, FD&C yellow no.5, FD&C yellow no.6, glycerin, methylchloroisothiazolinone, methylisothiazolinone, mineral oil, petrolatum, p glycol, triethanolamine, tocopheryl acetate, water

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  • Product Label
  • INGREDIENTS AND APPEARANCE
    LUCKY  DAILY MOISTURIZING
    dimethicone lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:20276-044
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 1 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:20276-044-12 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/31/2013
    2 NDC:20276-044-18 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/31/2013
    3 NDC:20276-044-08 227 mL in 1 TUBE; Type 0: Not a Combination Product 07/15/2016
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 01/31/2013
    Labeler - Delta Brands Inc (102672008)
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