Label: DIABETICS DRY SKIN RELIEF- dimethicone cream

  • NDC Code(s): 43689-0024-1, 43689-0024-2
  • Packager: The Magni Group Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 25, 2023

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

View All Sections
  • ​Drug Facts

  • ​Active ingredients (in cream)

    Dimethicone 1%

    ​Purpose

    Skin protectant

  • ​Uses

    • Helps prevent, relieve, and temporarily protects chafed, chapped, or cracked skin
    • Heps prevent and protect from the drying effects of wind and cold weather
  • ​Warnings

    ​For external use only

    Keep out of reach of children

    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

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

  • ​Directions

    • Apply as needed
  • ​Inactive ingredients

    Water (Aqua), Canola Oil, Ethylhexyl Stearate, Propylene Glycol, Beeswax, Tocopheryl Acetate, Ceteth-20, Cetyl Alcohol, Steareth-10, Steareth-21, Carbomer, Oleyl Lactate, Glyceryl Stearate, Stearic Acid, Phenoxyethanol, PEG-100 Stearate, Glycerin, Sodium Hydroxide, Citrullus Lanatus (Watermelon) Fruit Extract, Benzoic Acid, Urea, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Sorbic Acid, Sodium Lactate, Sodium PCA, Sea Salt, Plakton Extract, Ethyl Linoleate, Cucumis Sativus (Cucumber) Fruit Extract

  • Package Labels:

    BoxJar

  • INGREDIENTS AND APPEARANCE
    DIABETICS DRY SKIN RELIEF 
    dimethicone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43689-0024
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CANOLA OIL (UNII: 331KBJ17RK)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CETETH-20 (UNII: I835H2IHHX)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    STEARETH-10 (UNII: FD0913P475)  
    STEARETH-21 (UNII: 53J3F32P58)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    OLEYL LACTATE (UNII: B3AWW0N3GM)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATERMELON (UNII: 231473QB6R)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    UREA (UNII: 8W8T17847W)  
    LENS CULINARIS FRUIT (UNII: ZYZ076G9JH)  
    APPLE (UNII: B423VGH5S9)  
    SORBIC ACID (UNII: X045WJ989B)  
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    SEA SALT (UNII: 87GE52P74G)  
    ETHYL LINOLEATE (UNII: MJ2YTT4J8M)  
    CUCUMBER (UNII: YY7C30VXJT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43689-0024-1113 g in 1 JAR; Type 0: Not a Combination Product05/12/2017
    2NDC:43689-0024-21 in 1 BOX05/12/2017
    2113 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01605/12/2017
    Labeler - The Magni Group Inc (113501902)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!