Egolan Hand Sanitizer
FDA Label NDC 75448-025
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sanrace Biotechnology Co., Ltd. for the product Egolan Hand Sanitizer (NDC 75448-025). 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 drug facts, active ingredient, purpose, warnings, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 70%
Purpose
Antimicrobial
Warnings
For External use only. Flammable. Keep away from flames. Keep out of eyes. In case of contact with eyes, rinse eyes thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest. Stop use and contact doctor if irritation develops or persists for more than 72 hours.
Packaging
Image (Label75448)
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