Drugplain

Aluroderm Scar .0075 g/g

allantoin · PATCH · Olakino Therapeutics LLC

No Recall History
Plain English

Aluroderm Scar is a patch containing allantoin at .0075 g/g, taken cutaneous. Manufactured by Olakino Therapeutics LLC.

Key Facts

Brand Name
Aluroderm Scar
Generic Name
allantoin
NDC Code (Product)
84991-0316
Manufacturer
Olakino Therapeutics LLC
Strength
.0075 g/g
Dosage Form
PATCH
Route
CUTANEOUS
Marketing Status
Application #
M016
Marketing Start
12/24/2024

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

USES -Scar Management -Temporarily protects and helps relieve chapped or cracked skin

Dosage & Administration

DIRECTIONS Adults and Children 12 Years of Age and Older -Clean and dry the affected area -Apply as needed

Warnings

WARNINGS FOR EXTERNAL USE ONLY

Frequently Asked Questions

What is Aluroderm Scar used for?

Aluroderm Scar contains allantoin. It is a patch taken cutaneous. Consult your doctor for specific uses.

Is Aluroderm Scar a controlled substance?

Aluroderm Scar is not classified as a controlled substance by the DEA.

What is the generic name for Aluroderm Scar?

The generic name for Aluroderm Scar is allantoin. There are 10 other brand versions of allantoin.

What is the NDC code for Aluroderm Scar .0075 g/g?

The NDC (National Drug Code) for Aluroderm Scar .0075 g/g is 84991-0316, listed by Olakino Therapeutics LLC.