Otc - Active Ingredient
Alcohol 80% v/v
Alcohol
FDA Label NDC 74021-0008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bacardi Bottling Corporation for the product Alcohol (NDC 74021-0008). 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, otc - purpose, indications & usage, otc - do not use, otc - stop use, otc - keep out of reach of children, warnings, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
Indications & Usage
Health care personnel hand rub to help reduce bacteria that potentially can cause disease.
Otc - Do Not Use
• in children less than 2 months of age
• on open skin wounds
Otc - Stop Use
. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Warnings
For external use only. Flammable. Keep away from heat or flame
Dosage & Administration
Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.
Other Safety Information
Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredient
glycerin, hydrogen peroxide, purified water USP
* Please review the disclaimer below.
