Active Ingredient
Ethyl Alcohol 62%
Antibacterial Hand Sanitizer
FDA Label NDC 75613-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Lanzi Cosmetic Technology Co., Ltd for the product Antibacterial Hand Sanitizer (NDC 75613-002). 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, 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
Help reduce bacteria on skin.
Warnings
For external use only.
Flammable.Keep product away from fire or flame.
Do not use on damaged or broken skin.
Keep out of eye. In case of eye contact, immediately flush with water then contact physician.
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
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