Active Ingredient
Ethyl Alcohol 72% v/v
Hand Sanitizer
FDA Label NDC 75613-010
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 75613-010). 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
Hand sanitizer to Helps reduce bacteria that potentially can cause disease.
For use when soap and water are not available.
Warnings
For external use only: hands.
Flammable. Keep away from heat or flame.
Do not use
On children under the age of 2 months. On any open wounds.
When using this product
Keep out of eyes, ears, and mouth. In case of eye contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or redness occurs. These may be signs of serious reaction.
Other Information:
Store between 50-86℉ (15-30℃) 。
Avoid freezing and excessive heat above 104℉ (40℃).
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Place a dime size amount into hand. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallwing.
Inactive Ingredients
Carbmer, Fragrance, Glycerin, Propylene Glycol, Triethanolamine, Disodium ETDA, Tocopheryl Acetate, Deionized Water
* Please review the disclaimer below.
