Active Ingredient(S)
Alcohol 71% v/v
Instant Hand Sanitizer
FDA Label NDC 78413-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Foshan Kangkang Biotechnology?co.,ltd for the product Instant Hand Sanitizer (NDC 78413-001). 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, do not use, when using this product, stop use and ask a doctor, keep out of reach of children, 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 can cause disease
Warnings
For external use only; Do not eat ;Flammable,keep away from fire
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, 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.
Directions
Place enough product on hands to cover all surfaces. Rub hands together until dry.
Children under 6 years of age should be supervised when using this product.
Inactive Ingredients
Glycerin
* Please review the disclaimer below.
