Triderma Genuine Aloe Burn Cream
FDA Label NDC 10738-026

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Genuine Virgin Aloe Corporation for the product Triderma Genuine Aloe Burn (NDC 10738-026). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding warnings, active ingredient, keep out of reach of children., purpose, questions, stop use and ask a doctor before use, when using this product, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Warnings

For external use only.

Active Ingredient

Allantoin 1.5%

Keep Out Of Reach Of Children.

If swallowed, get medical help and contact a Poison Control Center right away.

Purpose

Skin Protectant

Questions

1-800-279-7282 M-F 8am-4pm PST

Stop Use And Ask A Doctor Before Use

in case of deep puncture wounds, animal bites or serious burns and if condition persists for more than 4 days or worsens.

When Using This Product

avoid contact with eyes. if contact occurs, rinse thoroughly with water

* Please review the disclaimer below.