MEDERMA FOR KIDS- allantoin gel 
HRA PHARMA AMERICA, INC.

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Mederma for kids DRUG FACTS

Active Ingredients

Allantoin 1%

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 or punctured 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, Xanthan Gum, Alcohol, Allium Cepa (Onion) Bulb Extract, Fragrance, Methylparaben, Sorbic Acid, Ext. Violet 2, Red 4, Sodium Chloride, Sodium Sulfate

Questions or Comments?

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

PRINCIPAL DISPLAY PANEL

MEDERMA® for Kids™

Clinically shown to visibly reduce the appearance of scars

For Ages 2+

goes on purple & rubs in clear

Unique Triple-Action Formula with kid-friendly scent

No 1 Pediatrician recommended scar brand

Skin Protectant

1 x GEL TUBE

NET WT. 0.7 0z (20g)

carton
MEDERMA FOR KIDS 
allantoin gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73302-202
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Allantoin (UNII: 344S277G0Z) (Allantoin - UNII:344S277G0Z) Allantoin1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Polyethylene Glycol 200 (UNII: R95B8J264J)  
Xanthan Gum (UNII: TTV12P4NEE)  
Alcohol (UNII: 3K9958V90M)  
Onion (UNII: 492225Q21H)  
Methylparaben (UNII: A2I8C7HI9T)  
Sorbic Acid (UNII: X045WJ989B)  
Ext. D&C Violet No. 2 (UNII: G5UX3K0728)  
Fd&C Red No. 4 (UNII: X3W0AM1JLX)  
Sodium Chloride (UNII: 451W47IQ8X)  
Sodium Sulfate (UNII: 0YPR65R21J)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73302-202-201 in 1 CARTON10/01/2020
120 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01610/01/2020
Labeler - HRA PHARMA AMERICA, INC. (081160441)

Revised: 11/2023
Document Id: 0bb4b095-da3b-4a45-a08a-89b359a9a9d0
Set id: e770129b-7ad1-4817-9b3c-d8aa2b9615b8
Version: 3
Effective Time: 20231102
 
HRA PHARMA AMERICA, INC.