Egolan
FDA Label NDC 75448-027
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 (NDC 75448-027). 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, uses, warnings, otc - keep out of reach of children, 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
Antiseptic
Uses
■ To decrease bacteria on the skin that could cause disease. ■ When water, soap, and towel are not available. ■ Recommended for repeated use.
Warnings
For external use only: hands.
Flammable. Keep away from fire or flame.
When using this product ■ Keep out of eyes, ears, or mouth. ■ In case of eye contact, flush eyes thoroughly with water. ■ Avoid contact with broken skin. ■ Do not inhale or ingest.
Stop use and ask a doctor if ■ redness or irritation develop ■ condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. ■ Children should be supervised by an adult when using this product. ■ If swallowed, get medical help or contact a Poison Control Center right away.
Packaging
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