Drug Facts Active Ingredients
Ethyl Alcohol 75%
Sani Pure Hand Sanitizer
FDA Label NDC 71712-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Wuxi Huoban Daily-use Chemicals Science And Technology Co., Ltd for the product Sani Pure Hand Sanitizer (NDC 71712-003). 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 drug facts active ingredients, purpose, directions:, inactive ingredients:, warning, otc - keep out of reach of children, other safety information, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Directions:
- Wet hands thoroughly with product
- briskly rub hands together
- supervise children under 6 years in the use of this product
Inactive Ingredients:
Aqua,Glycerin, Carbomer, Triethanolamine, Aloe Vera, Vitamine E
Warning
- Flammable, keep away from flame.
- Do not use in eyes. In case of ontact immediately flush eyes with water then contact physician.
- If swallowed, get medical help or contact a Poison Control Center
- For External Use Only.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Other Safety Information
- store at 20C to 25C (68 to 77F)
- may discolor certain fabrics
Indications & Usage
- for handwashing to decrease bacteria on the skin
- recommended for repeated use
* Please review the disclaimer below.
