Active Ingredient(S)
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 51414-912
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yuyao Jessie Commodity Co., Ltd. for the product Hand Sanitizer (NDC 51414-912). 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(s), purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label - principal display panel, 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 or flame,
When using this product keep out of eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
Stop use and ask a doctor if irritation develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. except under adult supervision.
If swallowed, get medical help or call a poison control center right away.
Directions
Wet hands thoroughly with product and allow to dry without wiping.
For children under 6 age use only under adult supervision.
Not recommended for infants.
Inactive Ingredients
Carborner,Fragrance,Glycerin,Propylene Glycol,TocopherylAcetate,Triethanolamine,Water.
Package Label - Principal Display Panel
1 (912)
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