Indications & Usage
To decrease bacteria on the skin that could cause disease. Recommended for repeated use.
70 Rubbing Ethyl Alcohol Liquid
FDA Label NDC 74375-050
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Iron Lab Sa De Cv for the product 70 Rubbing Ethyl Alcohol (NDC 74375-050). 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 indications & usage, otc - active ingredient, dosage & administration, warnings, otc - keep out of reach of children, otc - ask doctor, inactive ingredient, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
70 Ethyl Alcohol
70% Ethyl Alcohol
Dosage & Administration
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.
Warnings
For external use only: hands. Flammable, Keep away from fire of flame.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Otc - Ask Doctor
Irritation or redness develops. Condition persist for more than 72 hours.
Inactive Ingredient
Purified Water
Otc - Stop Use
Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
Otc - Purpose
Antiseptic Alcohol
Package Label.Principal Display Panel
70 Rubbing Alcohol
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