Active Ingredient
Ethyl Alcohol 70%
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 74835-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hangzhou Lookon Commodity Co., Ltd for the product Hand Sanitizer (NDC 74835-002). 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, uses, warnings, when use this product, stop use, 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
Antiseptic
Uses
For hand sanitizing to decrease bacteria on the skin, kills99% common germs
Warnings
Flammable: Keep away from flame or high heat.
For external Use only;
When Use This Product
When use this product avoid contact with the eyes.
Stop Use
Stop use and ask a doctor if irritation or redness develop
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
Rub a dime sized drop into hands
Inactive Ingredient
Aqua,Glycerin,Triethanolamine ,carbomer,vitamin E,Aloe Vera
Package Label
Hand Sanitizer
29ml
NDC: 74835-001-01
Hand Sanitizer
30ml
NDC: 74835-001-02
Hand Sanitizer
59ml
NDC: 74835-001-03
Hand Sanitizer
60ml
NDC: 74835-001-04
Hand Sanitizer
300ml
NDC: 74835-001-05
Hand Sanitizer
500ml
NDC: 74835-001-06
Hand Sanitizer
29ml
NDC: 74835-002-01
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