Otc - Active Ingredient
Ethyil Alcohol 75%
Hand Sanitizer Liquid
FDA Label NDC 87111-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Hudson Import& Export Co., Ltd for the product Hand Sanitizer (NDC 87111-001). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, otc - 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
Otc - Purpose
Antiseptic
Indications & Usage
Uses
Hand sanitizer to help decrease bacteria on the skin
When water, soap & towel are not available.
Recommended for repeated use.
Warnings
For external use only
Flammable
Keep away from fire or flame
Otc - Do Not Use
Do not apply around eyes.
Do not use in ears & mouth.
Otc - When Using
When using this product. avoid contact with eyes.
In case of contact flush eyes with water
Otc - Stop Use
Stop use and ask a doctor it redness or irritation develop and persist for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children must be supervised in use of this product
Dosage & Administration
Pump as needed into your palms and thoroughly spread on both hands. Rub into skin until dry
Inactive Ingredient
WATER
Tocopheryl Acetate
GLYERIN
Package Label.Principal Display Panel
Label1 (Label1)
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