Active Ingredient
Active ingredient
Ethyl Alcohol 80%
Baciban
FDA Label NDC 77330-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bonaventura Industries Inc for the product Baciban (NDC 77330-003). 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, do not use, when using this product, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Uses
Hand sanitizer to help reduce bacteria on the hands
Warnings
For external use only-hands.
Flammable. Keep away from heat and flame. Do not use in
children less than 2 months of age on open skin wounds
Do Not Use
- in children less than 2 months of age
- on open skin wounds
When Using This Product
Keep out of eyes, ears, and mouth.
In case of contact with eyes, flush thoroughly with water.
Directions
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 Information
•Store between 15-30C
• Avoid freezing and excessive heat above 40C (104F)
• may discolor some fabrics • harmful to wood finishes and plastics
Inactive Ingredients
Glycerin, Hydrogen Peroxide, Guaraprolose, Citric Acid, Purified Water USP
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help of contact a Poison Control Center immediately.
* Please review the disclaimer below.
