Active Ingredient
Alcohol 80%v/v.
Instant Hand Sanitizer
FDA Label NDC 75709-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Xi'an Explution Tech Co.,ltd. for the product Instant Hand Sanitizer (NDC 75709-002). 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, use, warnings, when using this product, otc - stop use, keep out of reach for 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 on skin.
Warnings
For external use only.
Flammable.Keep away from heat or flame.
When Using This Product
do not use on open skin Wounds.Keep out of eyes.ln.case of contact with eyes.rinse eyes thoroughly with water.
Use with caution if allergic to alcohoL.
Otc - Stop Use
Stop use and ask a doctor if irritation of rash appears and tasts.
Keep Out Of Reach For Children
If swallowed.get medical help or contact a Poison Control Center right away.
Directions
1.Pump enough amount of product in your palm to thoroughly spread on both hands.
2.Rub thoroughly over all surfaces of both hands.
3.Rub hands together briskly until dry.
Other Information
Store below 106°F.(41°C)
May discolor certain fabrics or surface.
Inactive Ingredients
glycerin.hydrogen peroxide, purified water.
* Please review the disclaimer below.
