Otc - Active Ingredient
91% Ethyl Alcohol
The following Structured Product Label (SPL) was submitted to the FDA by Iron Lab Sa De Cv for the product Ethyl Rubbing Alcohol (NDC 74375-020). 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 otc - active ingredient, dosage & administration, instructions for use, inactive ingredient, otc - stop use, otc - purpose, warnings, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
91% Ethyl Alcohol
Thoroughly cover your hands with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product. Not recommended for infants.
Thoroughly cover your hands with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product. Not recommended for infants.
Purified Water
Irritation or redness develops. Condition persist for more than 72 hours.
To decrease bacteria on the skin that could cause disease. Recommended for repeated use.
For external use only: hands. Flammable, Keep away from fire of flame.
If swallowed, get medical help or contact a Poison Control Center right away
Irritation or redness develops. Condition persist for more than 72 hours.
Store below 105°F. May discolor some fabrics. Harmful to wood finishes and plastic
Thoroughly cover your hands with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product. Not recommended for infants.
Ethyl Rubbing Alcohol 91
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