Label: BATH AND BEAUTY DIABETICS FOOT CREAM- dimethicone, petrolatum lotion

  • 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 March 10, 2021

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

View All Sections
  • ACTIVE INGREDIENT

    Active Ingredient Purpose

    Dimethicone 1% ...... Skin Protectant

    Petrolatum 30%........Skin Protectant

  • PURPOSE

    Skin protectant

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • INDICATIONS & USAGE

    Use help prevent and temporarily protets chafed, chapped, or cracked skin.

  • WARNINGS

    Warnings For external use only.

    When using this product

    avoid contact with eyes. In case of eye contact, flush with water.

    Do not use on

    Do not use on

    deep or puncture wounds
    animal bites
    serious burns

    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.

  • DOSAGE & ADMINISTRATION

    Directions  apply liberally as often as needed.

  • OTHER SAFETY INFORMATION

    Other information Store at room temperature.

  • INACTIVE INGREDIENT

    Inactive Ingredients Water, Ceterayl Alcohol, PEG-100 Stearate, Glycerin, Glyceryl Stearate, Polyquaternium-22, C13-16 Isoparaffin Laureth-25,DMDM Hydantoin, Carbomer, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Panthenol, Tocopheryl Acetate

  • PRINCIPAL DISPLAY PANEL

    5

  • INGREDIENTS AND APPEARANCE
    BATH AND BEAUTY  DIABETICS FOOT CREAM
    dimethicone, petrolatum lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76772-026
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM30 g  in 100 g
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    C13-16 ISOPARAFFIN (UNII: LED42LZG6O)  
    LAURETH-7 (UNII: Z95S6G8201)  
    POLYQUATERNIUM-22 (4500 MPA.S) (UNII: H3W1D31JAR)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    LAURETH-25 (UNII: RPD53041LR)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76772-026-11113 g in 1 TUBE; Type 0: Not a Combination Product03/10/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34703/10/2021
    Labeler - TSM ITHALAT IHRACAT SANAYI VE DIS TICARET LIMITED SIRKETI (533120570)
    Registrant - TSM ITHALAT IHRACAT SANAYI VE DIS TICARET LIMITED SIRKETI (533120570)
    Establishment
    NameAddressID/FEIBusiness Operations
    TSM ITHALAT IHRACAT SANAYI VE DIS TICARET LIMITED SIRKETI533120570manufacture(76772-026)
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!