Active Ingredient(S)
Isopropyl Alcohol 70% v/v. Purpose: Antiseptic
Vanitizer I-200
FDA Label NDC 47643-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vantage Specialties Ingredients, Inc for the product Vanitizer I-200 (NDC 47643-008). 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(s), uses, warnings, do not use, directions, other information, inactive ingredients, keep out of reach of childern, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only.
Flammable. Keep away from heat or flame.
When using this product keep out of eyes, ears and mouth. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Do Not Use
in children less than 2 months of age
on open skin wounds
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 (59-86F)
Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
glycerin, purified water USP, hydroxypropyl cellulose
Keep Out Of Reach Of Childern
If swallowed, get medical help or contact a Poison Control Center right away.
* Please review the disclaimer below.
