Label: TERRASIL FOOT ULCER AND SORE RELIEF- allantoin ointment

  • NDC Code(s): 24909-044-44, 24909-044-85
  • Packager: Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 21, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active ingredients

    Allantoin 0.6%

  • Purpose

    Skin Protectant

  • Uses

    Helps prevent, temporarily protect, and relieve chapped or cracked skin.

  • 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. Consult a doctor before using on deep or puncture wounds, animal bites or serious burns.

    Keep out of reach of children.

    If swallowed, call Poison Control or seek medical help.

  • Directions

    Wash and dry affected skin. Apply an ample amount of ointment. Cover with a clean bandage. Repeat procedure 1 to 3 times daily until skin improves or as directed by a doctor. Store at room temperature. May temporarily (washable) discolor skin and fabrics in
    sunlight.

  • Inactive ingredients

    beeswax, calendula extract, coconut oil (organic), comfrey extract, cottonseed oil*, jojoba oil, magnesium oxide, MCT oil, peppermint oil, sage oil, silver stearate, sunflower oil*, tea tree oil, thuja extract, vegetable stearic acid (naturally sourced)*, zinc oxide

    *May contain this ingredient

  • PRINCIPAL DISPLAY PANEL

    Image

  • INGREDIENTS AND APPEARANCE
    TERRASIL FOOT ULCER AND SORE RELIEF 
    allantoin ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24909-044
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.6 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    COCONUT OIL (UNII: Q9L0O73W7L)  
    PALM OIL (UNII: 5QUO05548Z)  
    SILVER STEARATE (UNII: 4H6PCL92ZN)  
    THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    COTTONSEED OIL (UNII: H3E878020N)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    MAGNESIUM OXIDE (UNII: 3A3U0GI71G)  
    SAGE OIL (UNII: U27K0H1H2O)  
    JOJOBA OIL (UNII: 724GKU717M)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    COMFREY ROOT (UNII: M9VVZ08EKQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24909-044-4444 g in 1 JAR; Type 0: Not a Combination Product12/15/2024
    2NDC:24909-044-8585 g in 1 TUBE; Type 0: Not a Combination Product12/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/15/2024
    Labeler - Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions (018950611)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions018950611manufacture(24909-044) , label(24909-044)
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

More Info on this Drug

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