Active Ingredient
Ethyl Alcohol 85 % v/v
Sterillium Foam Liquid
FDA Label NDC 65616-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bode Chemie Gmbh for the product Sterillium Foam (NDC 65616-006). 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, otc - do not use, otc - stop use, otc - 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 handwashing to decrease bacteria on the skin.
- Recommended for repeated use.
Warnings
For external use only.
Flammable, keep away from fire or flame.
Otc - Do Not Use
Do not use in or near the eyes or on mucous membranes.
In case of contact, rinse thoughly with water.
Otc - Stop Use
Stop use and ask a doctor if
- irritation and redness develop
- conditions persists for more than 72 hours
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.
Directions
- Apply to clean, dry hands, covering entire surface, including nails
- Rub until dry
- Supervise children in the use of this product
Inactive Ingredients
Bis-PEG/PPG-20/20 Dimethicone, Cyclomethicone, Glycerin, Isopropyl Alcohol, Myristyl Alcohol, Water.
* Please review the disclaimer below.
