Active Ingredient
Ethyl Alcohol 68%
Hand Sanitizer
FDA Label NDC 75613-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Lanzi Cosmetic Technology Co., Ltd for the product Hand Sanitizer (NDC 75613-008). 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, purpose, use, warnings, keep out of reach of children., directions, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For hand sanitizing
Warnings
For external use only.
Flammable.Keep away from heat and flame.
When using this product
keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Avoid contact with broken skin.
Stop use and ask a doctor if
rash occurs.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wet hands thoroughly with product and rub hands together briskly until dry.
Inactive Ingredients
Glycerin,Propylene Glycol, Triethanolamine, Carbomer, Fragrance, Disodium Edta, Tocopheryl Acetate, Deionized Water
* Please review the disclaimer below.
