MEDERMA ADVANCED SCAR- allantoin gel 
HRA PHARMA AMERICA, INC.

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MEDERMA® Advanced Scar Gel DRUG FACTS

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
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)

Revised: 11/2023
Document Id: 9b5b78ea-3d72-4078-acc0-b58f59b03a16
Set id: 25bc1eae-3502-4c63-bd8a-43be2dfb0d6d
Version: 4
Effective Time: 20231103
 
HRA PHARMA AMERICA, INC.