Dosage & Administration
Store in a cool dry place.
Instant Hand Sanitizer
FDA Label NDC 55422-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Keruisi Cosmetics (jinhua) Co.,ltd. for the product Instant Hand Sanitizer (NDC 55422-005). 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 dosage & administration, inactive ingredient, indications & usage, otc - active ingredient, otc - keep out of reach of children, otc - purpose, warnings, 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
Inactive Ingredient
AQUA
Propylene Glycol
Glycerin
CARBOMER
AMINOMETHYL PROPANOL
Indications & Usage
apply approptiate amount of this product to The palm.rub with both hands until dry without washing.
Otc - Active Ingredient
ALCOHOL
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Purpose
Disinfection
Sterilization
Warnings
1 keep out of reach of children.cont be swallowed just for External disinfectant.
2.Avoid to use together with agonist drugs.
3.Use in coution if allegric.
4.Flammable liquid.keep product away from heal.
5.Store in a cool dry place.
6.Always seals after use before Validity period.
Package Label.Principal Display Panel
Label (Label)
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