Egolan
FDA Label NDC 75448-024
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 75448-024). 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, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 75%
Purpose
Antiseptic
Warnings
Flammable. Keep away from fire or flame.
For external use only. do not inhale or ingest.
Do not use in, or near the eyes. In case of contact with eyes, rinse thoroughly with water.
Avoid contact with broken skin.
Stop use and ask a doctor if irritation or rash develops and persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
• Wet hands thoroughly with product and allow to dry without wiping.
• For children under 6, use only under adult supervision.
• Not recommended for infants
Other Information
• Store at room temperature (66°F-77°F)
• May discolor certain fabrics or surfaces
Inactive Ingredients
Water, Aloe Vera Gel, Disodium EDTA
Packaging
Image1 (San1)
Image2 (San2)
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