Active Ingredient(S)
Alcohol 70% v/v.
Hand Sanitizer
FDA Label NDC 70146-012
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dr.sankunnis Ayurvedic Research Foundation Pvt Ltd for the product Hand Sanitizer (NDC 70146-012). 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), purpose, use, warnings, otc - when using, 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
Antimicrobial
Use
Hand Sanitizer to help reduce bacteria that potentially could cause disease. Recommended for repeated use
Warnings
For external use only. Flammable. Keep away from heat or flame
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
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.
Directions
- Place enough product on hands to cover your hands. Rub hands briskly until dry.
- No rinsing required
- No towels needed
Other Information
- Do not store above 110F (43C)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Vitamin E, Demineralized Water, Glycerin
* Please review the disclaimer below.
