Active Ingredient
Ethyl Alcohol 70%
Ethanol Gel
FDA Label NDC 82442-031
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation Inc. for the product Ethanol (NDC 82442-031). 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 active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For personal hand hygiene to help prevent the spread of bacteria, and can be used in place of hand washing if soap and water are not available.
Warnings
For External use only.
- Flammable.
- Keep away from source of heat or fire.
When Using This Product
- Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
- Do not inhale or ingest.
Stop Use And Ask A Doctor If
- irritation or redness develops and lasts.
Keep Out Of Reach Of Children
In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.
Directions
- For occassional and personal use.
- Rub thoroughly into hands for at least 30 seconds. Allow to dry.
- Children under 6 should only use the product under adult supervision.
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Tocopheryl Acetate, Water (Aqua).
Questions?
1-800-910-6874.
Principal Display Panel
Principal Display Panel (Pdp 1)
* Please review the disclaimer below.
