Label: MEDERMA ADVANCED SCAR- allantoin gel

  • NDC Code(s): 73302-201-20, 73302-201-50
  • Packager: HRA PHARMA AMERICA, INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 3, 2023

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

View All Sections
  • Active Ingredients

    Allantoin 0.5%

  • Purpose

    Skin Protectant

  • Uses

    •
    Temporarily protects and helps 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

    Do not use on

    •
    Deep 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
  • Other Information

    •
    Store at room temperature
  • Inactive Ingredients

    •
    Water, PEG-4, Alcohol, Xanthan Gum, Allium Cepa (Onion) Bulb Extract, Panthenol, Fragrance, Lecithin, Methylparaben, Sorbic Acid, Sodium Hyaluronate
  • Questions or Comments?

    •
    For more information call 1-833-426-6733 or visit www.mederma.com
  • PRINCIPAL DISPLAY PANEL

    MEDERMA® ADVANCED SCAR GEL 

    Clinically shown to visibly reduce the appearance of scars

    No 1 Doctor & Pharmacist recommended scar brand

    Skin Protectant

    1 x GEL TUBE

    NET WT. 1.76 Oz (50g)

    Unique Triple-Action Formula penetrates into the skin

    carton
  • INGREDIENTS AND APPEARANCE
    MEDERMA ADVANCED SCAR 
    allantoin gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73302-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Allantoin (UNII: 344S277G0Z) (Allantoin - UNII:344S277G0Z) Allantoin5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Polyethylene Glycol 200 (UNII: R95B8J264J)  
    Alcohol (UNII: 3K9958V90M)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Onion (UNII: 492225Q21H)  
    Sorbic Acid (UNII: X045WJ989B)  
    Panthenol (UNII: WV9CM0O67Z)  
    Egg Phospholipids (UNII: 1Z74184RGV)  
    Methylparaben (UNII: A2I8C7HI9T)  
    Hyaluronate Sodium (UNII: YSE9PPT4TH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73302-201-201 in 1 BOX11/01/2013
    120 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:73302-201-501 in 1 BOX11/01/2013
    250 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01611/01/2013
    Labeler - HRA PHARMA AMERICA, INC. (081160441)
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!