Active Ingredients
ISOPROPYL ALCOHOL - 75% v/v ..............................................(Antiseptic)
Isopropyl Alcohol
FDA Label NDC 83290-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Amtime, Inc. for the product Isopropyl Alcohol (NDC 83290-001). 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 ingredients, use, indications & usage, warning, otc - keep out of reach of children, do not use, stop use and ask a doctor if, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use
Hand sanitizer to decrease bacteria on the skin.
Recommended for repeated use.
Indications & Usage
Clean hands to avoid bacterial infection
Warning
For extenal use only.
Flammable. Keep away from fire or flame.
Otc - Keep Out Of Reach Of Children
keep out of reach of children.
Do Not Use
Do not use in or near the eyes. lf contact occurs, rinse thoroughly with water.
Stop Use And Ask A Doctor If
Rash or irritation develops and lasts more than 24 hrs.
lf swallowed , get medical help or contact a Poison ControlCenter immediately.
Dosage & Administration
Rub hands thoroughly with product.
Rub hands together until dry.
Children under 6 years of age should be supervised whenusing this product.
Inactive Ingredients
ALOE VERA LEAF, CHAMOMILE, PROPYLENE GLYCOL, TOCOPHEROL, WATER
Other Information
Store at room temperature 68°F to 77°F(20° to 25°C).
Do not expose to heat or open flame. May discolor certain fabrics.
* Please review the disclaimer below.
