Active Ingredient
Ethy Alcohol 75%
Hand Sanitizer
FDA Label NDC 78019-800
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Wenzhou Shengkai Technology Industry Co., Ltd. for the product Hand Sanitizer (NDC 78019-800). 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, 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
Use:Help reduce bacteria that potentially can cause disease.
Warnings
For externaluse on/y. Flammable. Keep away from heat o1 flame.
Do not use
In children less than 2 months of age On open skin wounds.
Allergic to alcohol
When using this product
Keep out ofeyes, ears, and mouth./n case of contact with eyes,
rinse eyes thoroughly with water.
Stop use: stop use and ask a doctor if irritation or rash occurs
Otc - 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
Take out the product and spread it on your skin until dry.
Supervise children under 6 years of age when using this product to
avoid swallowing.
Inactive Ingredients
Water, Carbomer
* Please review the disclaimer below.
