Aluroderm Scar
allantoin · Patch · Cutaneous
Active ingredient
Allantoin 0.75%
Purpose
Skin Protectant
Uses
USES -Scar Management -Temporarily protects and helps relieve chapped or cracked skin
Warnings
WARNINGS FOR EXTERNAL USE ONLY
Do not use
DO NOT USE -On deep punctures, serious burns, or infected skin
When using this product
Avoid contact with the eyes
Stop use and ask a doctor
STOP USE AND ASK DOCTOR IF -Condition worsens -Excessive skin irritation develops -Condition persists for more than 7 days, or condition clears up and occurs again within 3 days
Pregnancy or breast-feeding
Consult a physician before use
Keep out of reach of children
If ingested, seek medical help or contact Poison Control immediately
Directions
Adults and Children 12 Years of Age and Older -Clean and dry the affected area -Apply as needed
Inactive ingredients
Hyaluronic Acid, Taxifolin, Polyurethane, Sodium Carboxymethyl Cellulose
Label text from the FDA structured product label by Olakino Therapeutics LLC (revised Feb 7, 2025). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Allantoin in 2 products
Aluroderm Scar NDC products (2)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 76420-955 | Allantoin .0075 g/g Patch | Asclemed USA, Inc. | OTC MONOGRAPH DRUG |
| 84991-0316 | Allantoin .0075 g/g Patch | Olakino Therapeutics LLC | OTC MONOGRAPH DRUG |
Frequently asked questions
What is Aluroderm Scar used for?
USES -Scar Management -Temporarily protects and helps relieve chapped or cracked skin
Who makes Aluroderm Scar?
Aluroderm Scar is listed by 2 labelers in the FDA NDC directory, including Asclemed USA, Inc., Olakino Therapeutics LLC.